ClinVar Miner

List of variants in gene FREM2 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 271
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HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.2128C>T (p.Arg710Cys) rs41292753 0.00274
NM_207361.6(FREM2):c.9113T>C (p.Val3038Ala) rs114688149 0.00204
NM_207361.6(FREM2):c.5642-9T>C rs148794835 0.00141
NM_207361.6(FREM2):c.2740T>G (p.Cys914Gly) rs146685625 0.00127
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met) rs114400765 0.00118
NM_207361.6(FREM2):c.7429C>T (p.Arg2477Trp) rs143571375 0.00115
NM_207361.6(FREM2):c.3539C>G (p.Pro1180Arg) rs139236965 0.00107
NM_207361.6(FREM2):c.5417G>A (p.Gly1806Asp) rs145208009 0.00101
NM_207361.6(FREM2):c.2367G>A (p.Pro789=) rs140101984 0.00095
NM_207361.6(FREM2):c.1580C>T (p.Ser527Leu) rs139804851 0.00084
NM_207361.6(FREM2):c.177T>C (p.Gly59=) rs370018440 0.00079
NM_207361.6(FREM2):c.2823C>T (p.Pro941=) rs150154438 0.00079
NM_207361.6(FREM2):c.7535G>A (p.Arg2512His) rs61978626 0.00058
NM_207361.6(FREM2):c.4991C>T (p.Ala1664Val) rs149779771 0.00051
NM_207361.6(FREM2):c.6664C>T (p.Pro2222Ser) rs137899618 0.00050
NM_207361.6(FREM2):c.8918A>G (p.Lys2973Arg) rs147506207 0.00047
NM_207361.6(FREM2):c.2754C>T (p.Val918=) rs140353326 0.00046
NM_207361.6(FREM2):c.4960A>C (p.Ser1654Arg) rs114595447 0.00046
NM_207361.6(FREM2):c.6201T>A (p.Asn2067Lys) rs114229197 0.00042
NM_207361.6(FREM2):c.181G>C (p.Ala61Pro) rs553605556 0.00032
NM_207361.6(FREM2):c.560C>T (p.Pro187Leu) rs200691357 0.00032
NM_207361.6(FREM2):c.2432G>A (p.Gly811Glu) rs147293913 0.00031
NM_207361.6(FREM2):c.6860T>C (p.Ile2287Thr) rs200983871 0.00029
NM_207361.6(FREM2):c.7062G>A (p.Thr2354=) rs41286130 0.00026
NM_207361.6(FREM2):c.826A>G (p.Asn276Asp) rs200898675 0.00026
NM_207361.6(FREM2):c.9009C>T (p.Val3003=) rs145657148 0.00026
NM_207361.6(FREM2):c.9356C>T (p.Thr3119Met) rs143100970 0.00024
NM_207361.6(FREM2):c.1677G>C (p.Gln559His) rs199921323 0.00021
NM_207361.6(FREM2):c.9418A>G (p.Ser3140Gly) rs199853872 0.00020
NM_207361.6(FREM2):c.1505C>T (p.Ser502Phe) rs202008233 0.00019
NM_207361.6(FREM2):c.4975G>A (p.Ala1659Thr) rs114440488 0.00019
NM_207361.6(FREM2):c.8906T>C (p.Leu2969Pro) rs140937193 0.00019
NM_207361.6(FREM2):c.4567C>T (p.Arg1523Cys) rs200817424 0.00018
NM_207361.6(FREM2):c.1345C>G (p.Leu449Val) rs190063725 0.00016
NM_207361.6(FREM2):c.2987T>A (p.Val996Asp) rs138416277 0.00016
NM_207361.6(FREM2):c.7366G>A (p.Asp2456Asn) rs138539682 0.00016
NM_207361.6(FREM2):c.2801G>A (p.Arg934Gln) rs145484598 0.00013
NM_207361.6(FREM2):c.4558C>T (p.Arg1520Trp) rs142322683 0.00013
NM_207361.6(FREM2):c.6421G>A (p.Glu2141Lys) rs376602370 0.00013
NM_207361.6(FREM2):c.6743-9C>T rs749834830 0.00013
NM_207361.6(FREM2):c.1737C>T (p.Ile579=) rs144811771 0.00012
NM_207361.6(FREM2):c.4150C>T (p.His1384Tyr) rs192340937 0.00012
NM_207361.6(FREM2):c.4886A>G (p.Tyr1629Cys) rs553816676 0.00012
NM_207361.6(FREM2):c.3143A>G (p.Asn1048Ser) rs115192563 0.00011
NM_207361.6(FREM2):c.7427C>T (p.Ser2476Phe) rs574419341 0.00011
NM_207361.6(FREM2):c.2075G>A (p.Arg692His) rs367642497 0.00010
NM_207361.6(FREM2):c.6333C>T (p.Gly2111=) rs116763572 0.00010
NM_207361.6(FREM2):c.6957C>A (p.His2319Gln) rs182710790 0.00009
NM_207361.6(FREM2):c.7883G>A (p.Arg2628Gln) rs199993718 0.00007
NM_207361.6(FREM2):c.1369C>G (p.Leu457Val) rs141900626 0.00006
NM_207361.6(FREM2):c.1647C>A (p.Phe549Leu) rs114341997 0.00006
NM_207361.6(FREM2):c.3785G>C (p.Ser1262Thr) rs753652530 0.00006
NM_207361.6(FREM2):c.5059G>T (p.Glu1687Ter) rs148965852 0.00006
NM_207361.6(FREM2):c.5060A>C (p.Glu1687Ala) rs143708269 0.00006
NM_207361.6(FREM2):c.6272C>T (p.Ala2091Val) rs374178459 0.00006
NM_207361.6(FREM2):c.7103A>T (p.Asp2368Val) rs760834204 0.00006
NM_207361.6(FREM2):c.8227G>A (p.Val2743Met) rs201978814 0.00006
NM_207361.6(FREM2):c.2093G>A (p.Arg698His) rs201217034 0.00005
NM_207361.6(FREM2):c.2596T>A (p.Phe866Ile) rs566743573 0.00005
NM_207361.6(FREM2):c.6807G>A (p.Ser2269=) rs752080876 0.00005
NM_207361.6(FREM2):c.8461C>G (p.Pro2821Ala) rs186980482 0.00005
NM_207361.6(FREM2):c.1394C>T (p.Pro465Leu) rs755744742 0.00004
NM_207361.6(FREM2):c.1921A>G (p.Thr641Ala) rs116802472 0.00004
NM_207361.6(FREM2):c.383C>T (p.Pro128Leu) rs114864077 0.00004
NM_207361.6(FREM2):c.38G>A (p.Arg13Gln) rs765718616 0.00004
NM_207361.6(FREM2):c.4823G>A (p.Gly1608Asp) rs767651775 0.00004
NM_207361.6(FREM2):c.5276T>C (p.Leu1759Ser) rs750450348 0.00004
NM_207361.6(FREM2):c.6004C>T (p.Pro2002Ser) rs372782469 0.00004
NM_207361.6(FREM2):c.8509C>T (p.Pro2837Ser) rs766715445 0.00004
NM_207361.6(FREM2):c.1250T>C (p.Leu417Pro) rs571694324 0.00003
NM_207361.6(FREM2):c.2207G>A (p.Arg736Gln) rs201173265 0.00003
NM_207361.6(FREM2):c.4283G>A (p.Gly1428Glu) rs369891021 0.00003
NM_207361.6(FREM2):c.4415C>T (p.Thr1472Met) rs141478658 0.00003
NM_207361.6(FREM2):c.6016G>C (p.Asp2006His) rs1231644914 0.00003
NM_207361.6(FREM2):c.6499C>T (p.Arg2167Trp) rs114837786 0.00003
NM_207361.6(FREM2):c.1284G>A (p.Met428Ile) rs746265965 0.00002
NM_207361.6(FREM2):c.2473G>A (p.Val825Met) rs757937131 0.00002
NM_207361.6(FREM2):c.362G>A (p.Arg121His) rs1320388887 0.00002
NM_207361.6(FREM2):c.4439C>T (p.Thr1480Met) rs773471950 0.00002
NM_207361.6(FREM2):c.4561A>C (p.Thr1521Pro) rs777697719 0.00002
NM_207361.6(FREM2):c.6109C>A (p.Leu2037Met) rs539893834 0.00002
NM_207361.6(FREM2):c.65C>T (p.Pro22Leu) rs1460573845 0.00002
NM_207361.6(FREM2):c.6740A>G (p.Asp2247Gly) rs766949299 0.00002
NM_207361.6(FREM2):c.9463C>T (p.Pro3155Ser) rs555402630 0.00002
NM_207361.6(FREM2):c.1142C>G (p.Ser381Cys) rs200453874 0.00001
NM_207361.6(FREM2):c.2053G>A (p.Gly685Arg) rs773636566 0.00001
NM_207361.6(FREM2):c.3086C>T (p.Ala1029Val) rs200459256 0.00001
NM_207361.6(FREM2):c.326T>C (p.Val109Ala) rs909150998 0.00001
NM_207361.6(FREM2):c.332A>T (p.Asp111Val) rs761430669 0.00001
NM_207361.6(FREM2):c.3712A>G (p.Ile1238Val) rs776875620 0.00001
NM_207361.6(FREM2):c.3830T>G (p.Phe1277Cys) rs1437152125 0.00001
NM_207361.6(FREM2):c.4172G>A (p.Arg1391Gln) rs1367167650 0.00001
NM_207361.6(FREM2):c.4360G>A (p.Glu1454Lys) rs1368509400 0.00001
NM_207361.6(FREM2):c.5500A>G (p.Arg1834Gly) rs1162992431 0.00001
NM_207361.6(FREM2):c.5689G>T (p.Val1897Phe) rs1213042816 0.00001
NM_207361.6(FREM2):c.5810C>T (p.Ser1937Phe) rs1020313300 0.00001
NM_207361.6(FREM2):c.6382C>T (p.Pro2128Ser) rs774766906 0.00001
NM_207361.6(FREM2):c.6852G>T (p.Lys2284Asn) rs772357847 0.00001
NM_207361.6(FREM2):c.7177G>A (p.Ala2393Thr) rs769767420 0.00001
NM_207361.6(FREM2):c.7441G>A (p.Ala2481Thr) rs759338792 0.00001
NM_207361.6(FREM2):c.8176+2dup rs779126010 0.00001
NM_207361.6(FREM2):c.8218C>T (p.Arg2740Cys) rs775185183 0.00001
NM_207361.6(FREM2):c.8342G>A (p.Arg2781His) rs756570666 0.00001
NM_207361.6(FREM2):c.8777A>G (p.Tyr2926Cys) rs1878414292 0.00001
NM_207361.6(FREM2):c.993C>G (p.Asp331Glu) rs767767229 0.00001
GRCh37/hg19 13q13.3(chr13:39448121-39527619)x1
NM_207361.6(FREM2):c.105_106delinsTT (p.Leu36Phe) rs1566101411
NM_207361.6(FREM2):c.1162C>A (p.Leu388Met)
NM_207361.6(FREM2):c.1166G>T (p.Arg389Leu)
NM_207361.6(FREM2):c.1192C>G (p.Pro398Ala) rs372777373
NM_207361.6(FREM2):c.1238A>T (p.Glu413Val) rs2138064285
NM_207361.6(FREM2):c.1288G>A (p.Val430Met)
NM_207361.6(FREM2):c.1343T>A (p.Ile448Asn)
NM_207361.6(FREM2):c.1349A>G (p.Tyr450Cys)
NM_207361.6(FREM2):c.1364G>A (p.Arg455Gln) rs1217298919
NM_207361.6(FREM2):c.1463G>A (p.Arg488Gln)
NM_207361.6(FREM2):c.1541_1542delinsGT (p.Ala514Gly) rs1566103099
NM_207361.6(FREM2):c.1610T>G (p.Val537Gly)
NM_207361.6(FREM2):c.1622G>T (p.Gly541Val)
NM_207361.6(FREM2):c.1671T>G (p.Asp557Glu) rs768299920
NM_207361.6(FREM2):c.1774G>T (p.Asp592Tyr) rs368864300
NM_207361.6(FREM2):c.1820C>T (p.Thr607Met)
NM_207361.6(FREM2):c.1823G>A (p.Gly608Glu) rs774621627
NM_207361.6(FREM2):c.1843A>G (p.Thr615Ala) rs2138065634
NM_207361.6(FREM2):c.184G>T (p.Gly62Trp)
NM_207361.6(FREM2):c.1879G>A (p.Gly627Ser)
NM_207361.6(FREM2):c.2099C>A (p.Pro700His)
NM_207361.6(FREM2):c.2216G>A (p.Arg739His)
NM_207361.6(FREM2):c.2308G>T (p.Val770Leu) rs7327915
NM_207361.6(FREM2):c.2369G>T (p.Gly790Val)
NM_207361.6(FREM2):c.2383G>A (p.Val795Met)
NM_207361.6(FREM2):c.2404T>A (p.Phe802Ile)
NM_207361.6(FREM2):c.253C>T (p.Arg85Cys) rs975501544
NM_207361.6(FREM2):c.2620C>T (p.His874Tyr)
NM_207361.6(FREM2):c.2710C>T (p.His904Tyr)
NM_207361.6(FREM2):c.2794A>T (p.Asn932Tyr)
NM_207361.6(FREM2):c.2812G>A (p.Asp938Asn)
NM_207361.6(FREM2):c.2890A>G (p.Ile964Val)
NM_207361.6(FREM2):c.2912G>T (p.Gly971Val)
NM_207361.6(FREM2):c.2918A>T (p.Asn973Ile)
NM_207361.6(FREM2):c.3035_3040dup (p.Gly1012_Ser1013dup) rs570476408
NM_207361.6(FREM2):c.304G>C (p.Gly102Arg) rs1869535237
NM_207361.6(FREM2):c.3052C>G (p.His1018Asp)
NM_207361.6(FREM2):c.305G>C (p.Gly102Ala)
NM_207361.6(FREM2):c.3074T>C (p.Leu1025Pro)
NM_207361.6(FREM2):c.307G>C (p.Asp103His)
NM_207361.6(FREM2):c.3082A>G (p.Lys1028Glu)
NM_207361.6(FREM2):c.317C>T (p.Ala106Val)
NM_207361.6(FREM2):c.3245A>C (p.Lys1082Thr)
NM_207361.6(FREM2):c.3316A>G (p.Ile1106Val)
NM_207361.6(FREM2):c.3317T>C (p.Ile1106Thr)
NM_207361.6(FREM2):c.331G>A (p.Asp111Asn) rs1448740276
NM_207361.6(FREM2):c.3331A>G (p.Thr1111Ala)
NM_207361.6(FREM2):c.3341A>G (p.Tyr1114Cys)
NM_207361.6(FREM2):c.3496C>T (p.Arg1166Cys)
NM_207361.6(FREM2):c.3583A>G (p.Met1195Val)
NM_207361.6(FREM2):c.3612G>A (p.Met1204Ile)
NM_207361.6(FREM2):c.3629C>T (p.Thr1210Ile)
NM_207361.6(FREM2):c.3682A>G (p.Thr1228Ala)
NM_207361.6(FREM2):c.3703C>G (p.His1235Asp)
NM_207361.6(FREM2):c.3715A>T (p.Met1239Leu)
NM_207361.6(FREM2):c.3782C>T (p.Ser1261Phe)
NM_207361.6(FREM2):c.3790A>T (p.Ile1264Phe)
NM_207361.6(FREM2):c.3825C>G (p.Asp1275Glu)
NM_207361.6(FREM2):c.386G>T (p.Cys129Phe) rs745938776
NM_207361.6(FREM2):c.3883A>G (p.Ile1295Val)
NM_207361.6(FREM2):c.38G>T (p.Arg13Leu)
NM_207361.6(FREM2):c.3967A>C (p.Asn1323His) rs371827710
NM_207361.6(FREM2):c.4082T>C (p.Phe1361Ser)
NM_207361.6(FREM2):c.4321A>G (p.Thr1441Ala) rs886042127
NM_207361.6(FREM2):c.4325A>G (p.Asp1442Gly)
NM_207361.6(FREM2):c.4331T>C (p.Leu1444Pro) rs886042126
NM_207361.6(FREM2):c.4342G>A (p.Asp1448Asn)
NM_207361.6(FREM2):c.4350C>A (p.Asn1450Lys) rs1869872750
NM_207361.6(FREM2):c.4378A>G (p.Ile1460Val)
NM_207361.6(FREM2):c.437C>G (p.Pro146Arg)
NM_207361.6(FREM2):c.4430T>C (p.Val1477Ala) rs1319182599
NM_207361.6(FREM2):c.4474A>G (p.Ile1492Val) rs2138071590
NM_207361.6(FREM2):c.4537G>A (p.Asp1513Asn)
NM_207361.6(FREM2):c.4544G>A (p.Arg1515His)
NM_207361.6(FREM2):c.4568G>A (p.Arg1523His)
NM_207361.6(FREM2):c.4588G>C (p.Asp1530His) rs886043214
NM_207361.6(FREM2):c.4636A>G (p.Ser1546Gly)
NM_207361.6(FREM2):c.4688C>T (p.Thr1563Ile) rs772941769
NM_207361.6(FREM2):c.4829A>G (p.Glu1610Gly)
NM_207361.6(FREM2):c.4901C>A (p.Thr1634Lys) rs74781600
NM_207361.6(FREM2):c.5035A>C (p.Ile1679Leu)
NM_207361.6(FREM2):c.5059_5060inv (p.Glu1687Ser)
NM_207361.6(FREM2):c.5060A>G (p.Glu1687Gly)
NM_207361.6(FREM2):c.5120G>A (p.Gly1707Glu) rs886044224
NM_207361.6(FREM2):c.5148C>A (p.Asn1716Lys) rs2138073287
NM_207361.6(FREM2):c.5170C>G (p.Gln1724Glu)
NM_207361.6(FREM2):c.5209A>G (p.Arg1737Gly)
NM_207361.6(FREM2):c.5293C>T (p.Arg1765Cys)
NM_207361.6(FREM2):c.5294G>A (p.Arg1765His)
NM_207361.6(FREM2):c.5377C>T (p.Arg1793Cys)
NM_207361.6(FREM2):c.5434G>A (p.Ala1812Thr) rs749830746
NM_207361.6(FREM2):c.5581G>A (p.Val1861Met)
NM_207361.6(FREM2):c.5617G>A (p.Val1873Ile)
NM_207361.6(FREM2):c.5648C>A (p.Thr1883Asn)
NM_207361.6(FREM2):c.5677G>T (p.Val1893Phe)
NM_207361.6(FREM2):c.584G>A (p.Gly195Glu)
NM_207361.6(FREM2):c.5858A>G (p.Asp1953Gly) rs794727814
NM_207361.6(FREM2):c.5884C>T (p.Arg1962Trp)
NM_207361.6(FREM2):c.5946C>G (p.Ser1982Arg) rs2137831772
NM_207361.6(FREM2):c.5957G>A (p.Gly1986Glu)
NM_207361.6(FREM2):c.604G>C (p.Ala202Pro)
NM_207361.6(FREM2):c.6088G>C (p.Val2030Leu)
NM_207361.6(FREM2):c.6098C>T (p.Thr2033Met)
NM_207361.6(FREM2):c.6112T>A (p.Ser2038Thr)
NM_207361.6(FREM2):c.6177A>G (p.Thr2059=) rs794727940
NM_207361.6(FREM2):c.6292T>C (p.Phe2098Leu)
NM_207361.6(FREM2):c.6387G>C (p.Lys2129Asn)
NM_207361.6(FREM2):c.6404G>A (p.Arg2135Gln)
NM_207361.6(FREM2):c.6416G>A (p.Gly2139Asp)
NM_207361.6(FREM2):c.6458C>A (p.Thr2153Asn)
NM_207361.6(FREM2):c.6490T>C (p.Cys2164Arg) rs886042926
NM_207361.6(FREM2):c.6514C>G (p.Gln2172Glu)
NM_207361.6(FREM2):c.6547A>G (p.Thr2183Ala)
NM_207361.6(FREM2):c.6614A>G (p.Asp2205Gly)
NM_207361.6(FREM2):c.6674A>G (p.Asn2225Ser) rs143576067
NM_207361.6(FREM2):c.6718A>G (p.Ile2240Val)
NM_207361.6(FREM2):c.6728G>A (p.Arg2243Gln)
NM_207361.6(FREM2):c.685C>T (p.Arg229Cys)
NM_207361.6(FREM2):c.689A>G (p.Tyr230Cys) rs1869573182
NM_207361.6(FREM2):c.6947A>T (p.Glu2316Val) rs2137916746
NM_207361.6(FREM2):c.6958G>A (p.Val2320Met)
NM_207361.6(FREM2):c.6959T>G (p.Val2320Gly)
NM_207361.6(FREM2):c.7002_7005del (p.Glu2335fs) rs768342700
NM_207361.6(FREM2):c.7021C>G (p.Leu2341Val)
NM_207361.6(FREM2):c.7136C>G (p.Ser2379Cys)
NM_207361.6(FREM2):c.7193G>T (p.Gly2398Val)
NM_207361.6(FREM2):c.7264G>A (p.Ala2422Thr)
NM_207361.6(FREM2):c.7294C>T (p.Arg2432Trp)
NM_207361.6(FREM2):c.7329T>A (p.Pro2443=) rs1303270704
NM_207361.6(FREM2):c.7333G>A (p.Gly2445Ser)
NM_207361.6(FREM2):c.7378A>G (p.Thr2460Ala)
NM_207361.6(FREM2):c.7462A>G (p.Asn2488Asp) rs1877687604
NM_207361.6(FREM2):c.7490G>A (p.Ser2497Asn)
NM_207361.6(FREM2):c.7520-10_7520-9insCT rs1399473815
NM_207361.6(FREM2):c.7533C>T (p.Pro2511=)
NM_207361.6(FREM2):c.7652G>C (p.Gly2551Ala)
NM_207361.6(FREM2):c.7760C>T (p.Thr2587Ile)
NM_207361.6(FREM2):c.7817T>C (p.Ile2606Thr)
NM_207361.6(FREM2):c.7873C>A (p.Arg2625Ser) rs115492820
NM_207361.6(FREM2):c.7924T>C (p.Tyr2642His)
NM_207361.6(FREM2):c.8024C>T (p.Pro2675Leu) rs1357205318
NM_207361.6(FREM2):c.8201G>A (p.Arg2734His)
NM_207361.6(FREM2):c.8206G>A (p.Gly2736Ser) rs368732492
NM_207361.6(FREM2):c.8341C>T (p.Arg2781Cys)
NM_207361.6(FREM2):c.8381A>C (p.Gln2794Pro) rs2137937738
NM_207361.6(FREM2):c.8479C>T (p.Arg2827Cys)
NM_207361.6(FREM2):c.850G>C (p.Val284Leu) rs770004356
NM_207361.6(FREM2):c.8587A>G (p.Met2863Val)
NM_207361.6(FREM2):c.8612T>C (p.Leu2871Pro) rs1566175991
NM_207361.6(FREM2):c.87GCT[8] (p.Leu38_Ser39insLeu)
NM_207361.6(FREM2):c.881G>A (p.Gly294Asp) rs1869591293
NM_207361.6(FREM2):c.8882A>G (p.Gln2961Arg)
NM_207361.6(FREM2):c.8933A>T (p.Asp2978Val)
NM_207361.6(FREM2):c.9019C>T (p.Arg3007Ter)
NM_207361.6(FREM2):c.9056C>T (p.Ser3019Leu)
NM_207361.6(FREM2):c.9092G>A (p.Ser3031Asn)
NM_207361.6(FREM2):c.9140C>A (p.Thr3047Asn)
NM_207361.6(FREM2):c.9226C>A (p.Gln3076Lys) rs748307174
NM_207361.6(FREM2):c.9239T>C (p.Leu3080Pro) rs2137942953
NM_207361.6(FREM2):c.9316A>G (p.Ser3106Gly)
NM_207361.6(FREM2):c.9346G>A (p.Gly3116Arg)
NM_207361.6(FREM2):c.9415G>A (p.Glu3139Lys)
NM_207361.6(FREM2):c.9452G>C (p.Ser3151Thr)
NM_207361.6(FREM2):c.9500C>T (p.Ser3167Leu)
NM_207361.6(FREM2):c.996G>C (p.Gln332His)

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