ClinVar Miner

List of variants in gene FREM2 reported as benign by Invitae

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Gene type:
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Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_207361.6(FREM2):c.2233= (p.Pro745=) rs2496423 0.99994
NM_207361.6(FREM2):c.576G>A (p.Glu192=) rs1868464 0.99992
NM_207361.6(FREM2):c.6977C>T (p.Thr2326Ile) rs9548509 0.73365
NM_207361.6(FREM2):c.3209T>C (p.Phe1070Ser) rs2496425 0.43515
NM_207361.6(FREM2):c.7398A>G (p.Thr2466=) rs9532292 0.39041
NM_207361.6(FREM2):c.7984-10G>A rs9532295 0.19705
NM_207361.6(FREM2):c.8282-20A>C rs1945510 0.19704
NM_207361.6(FREM2):c.1542C>T (p.Ala514=) rs12874397 0.18215
NM_207361.6(FREM2):c.5518C>T (p.Arg1840Trp) rs9603422 0.14074
NM_207361.6(FREM2):c.2250C>T (p.Asp750=) rs41292755 0.07615
NM_207361.6(FREM2):c.2602C>G (p.Leu868Val) rs7329939 0.06144
NM_207361.6(FREM2):c.2165G>A (p.Arg722Lys) rs58363253 0.06139
NM_207361.6(FREM2):c.303C>A (p.Pro101=) rs8002488 0.05332
NM_207361.6(FREM2):c.5003G>A (p.Arg1668His) rs1868463 0.05268
NM_207361.6(FREM2):c.1941C>T (p.Asp647=) rs41292751 0.02517
NM_207361.6(FREM2):c.4077T>A (p.Gly1359=) rs41292757 0.02517
NM_207361.6(FREM2):c.8226C>T (p.Ala2742=) rs17058710 0.02172
NM_207361.6(FREM2):c.8885C>T (p.Ala2962Val) rs7996253 0.02012
NM_207361.6(FREM2):c.6606G>A (p.Glu2202=) rs61749310 0.01827
NM_207361.6(FREM2):c.9429G>A (p.Gly3143=) rs41306662 0.01662
NM_207361.6(FREM2):c.3116T>A (p.Met1039Lys) rs2496424 0.01608
NM_207361.6(FREM2):c.5642-19A>G rs77863177 0.01566
NM_207361.6(FREM2):c.954C>G (p.Pro318=) rs9576597 0.01462
NM_207361.6(FREM2):c.6339C>T (p.Pro2113=) rs116383837 0.00953
NM_207361.6(FREM2):c.6036C>T (p.Phe2012=) rs115455037 0.00893
NM_207361.6(FREM2):c.4901C>T (p.Thr1634Met) rs74781600 0.00872
NM_207361.6(FREM2):c.3753C>T (p.Ser1251=) rs78099370 0.00823
NM_207361.6(FREM2):c.1518C>T (p.Ser506=) rs141821695 0.00784
NM_207361.6(FREM2):c.6989T>C (p.Val2330Ala) rs61744595 0.00751
NM_207361.6(FREM2):c.1188G>C (p.Gln396His) rs61997174 0.00747
NM_207361.6(FREM2):c.5264-19T>G rs112155555 0.00631
NM_207361.6(FREM2):c.2978A>G (p.Glu993Gly) rs61742843 0.00597
NM_207361.6(FREM2):c.6330T>G (p.Leu2110=) rs112083916 0.00535
NM_207361.6(FREM2):c.6396C>T (p.Phe2132=) rs61745902 0.00525
NM_207361.6(FREM2):c.2600C>T (p.Thr867Ile) rs61995710 0.00520
NM_207361.6(FREM2):c.4031G>A (p.Arg1344His) rs143044921 0.00430
NM_207361.6(FREM2):c.7068C>T (p.Ala2356=) rs74577582 0.00410
NM_207361.6(FREM2):c.4730T>C (p.Ile1577Thr) rs114798977 0.00408
NM_207361.6(FREM2):c.4726C>G (p.Pro1576Ala) rs116742938 0.00406
NM_207361.6(FREM2):c.3979T>A (p.Leu1327Ile) rs116653247 0.00384
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile) rs116099212 0.00379
NM_207361.6(FREM2):c.6925+7G>T rs79530106 0.00364
NM_207361.6(FREM2):c.4319C>A (p.Thr1440Lys) rs79048205 0.00348
NM_207361.6(FREM2):c.5642-12T>C rs144415935 0.00329
NM_207361.6(FREM2):c.8460C>G (p.Ala2820=) rs138775857 0.00325
NM_207361.6(FREM2):c.9266A>G (p.His3089Arg) rs76949956 0.00279
NM_207361.6(FREM2):c.7335T>C (p.Gly2445=) rs141921562 0.00276
NM_207361.6(FREM2):c.5354A>C (p.Lys1785Thr) rs116599611 0.00248
NM_207361.6(FREM2):c.84C>G (p.Pro28=) rs141718695 0.00194
NM_207361.6(FREM2):c.4686T>C (p.Asp1562=) rs17058435 0.00172
NM_207361.6(FREM2):c.714G>A (p.Gln238=) rs116236946 0.00150
NM_207361.6(FREM2):c.5544G>A (p.Glu1848=) rs114674141 0.00141
NM_207361.6(FREM2):c.2740T>G (p.Cys914Gly) rs146685625 0.00127
NM_207361.6(FREM2):c.5109C>T (p.Ala1703=) rs11619157 0.00096
NM_207361.6(FREM2):c.2367G>A (p.Pro789=) rs140101984 0.00095
NM_207361.6(FREM2):c.8671+14A>G rs182974545 0.00088
NM_207361.6(FREM2):c.8757A>G (p.Leu2919=) rs144702001 0.00086
NM_207361.6(FREM2):c.690T>C (p.Tyr230=) rs115830086 0.00080
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.4916G>A (p.Arg1639Lys) rs77886481 0.00073
NM_207361.6(FREM2):c.3908C>T (p.Thr1303Met) rs138477887 0.00063
NM_207361.6(FREM2):c.6020-13C>T rs200860319 0.00022
NM_207361.6(FREM2):c.2180G>A (p.Arg727His) rs201714905 0.00021
NM_207361.6(FREM2):c.8172T>A (p.Leu2724=) rs201065518 0.00016
NM_207361.6(FREM2):c.9337A>G (p.Thr3113Ala) rs202106776 0.00014
NM_207361.6(FREM2):c.6669A>G (p.Gln2223=) rs114333791 0.00012
NM_207361.6(FREM2):c.5790G>A (p.Pro1930=) rs114346379 0.00010
NM_207361.6(FREM2):c.9238C>T (p.Leu3080=) rs138154238 0.00009
NM_207361.6(FREM2):c.7359G>A (p.Val2453=) rs115054860 0.00007
NM_207361.6(FREM2):c.1395G>A (p.Pro465=) rs181720619 0.00004
NM_207361.6(FREM2):c.1250T>C (p.Leu417Pro) rs571694324 0.00003
NM_207361.6(FREM2):c.6826G>A (p.Val2276Met) rs555028352 0.00002
NM_207361.6(FREM2):c.9184G>T (p.Ala3062Ser) rs140456319 0.00001
NM_207361.6(FREM2):c.9282A>C (p.Pro3094=) rs549071375 0.00001
NM_207361.6(FREM2):c.1122T>A (p.Asp374Glu)
NM_207361.6(FREM2):c.176G>A (p.Gly59Asp) rs115327344
NM_207361.6(FREM2):c.2062C>G (p.Arg688Gly) rs150928081
NM_207361.6(FREM2):c.2124C>G (p.Pro708=)
NM_207361.6(FREM2):c.2308G>A (p.Val770Met) rs7327915
NM_207361.6(FREM2):c.3035_3040dup (p.Gly1012_Ser1013dup) rs570476408
NM_207361.6(FREM2):c.3075A>G (p.Leu1025=)
NM_207361.6(FREM2):c.3738G>A (p.Thr1246=) rs530142447
NM_207361.6(FREM2):c.5173+20del
NM_207361.6(FREM2):c.5264-10dup
NM_207361.6(FREM2):c.5411-20_5411-18del rs751990950
NM_207361.6(FREM2):c.5411-7del
NM_207361.6(FREM2):c.6169+18C>T
NM_207361.6(FREM2):c.6196C>T (p.Arg2066Cys) rs9548505
NM_207361.6(FREM2):c.6379+19del
NM_207361.6(FREM2):c.6380-5dup
NM_207361.6(FREM2):c.6458_6459delinsGC (p.Thr2153Ser) rs35252750
NM_207361.6(FREM2):c.6577+24del rs748216447
NM_207361.6(FREM2):c.6657C>T (p.Leu2219=)
NM_207361.6(FREM2):c.6674A>G (p.Asn2225Ser) rs143576067
NM_207361.6(FREM2):c.6742+17del rs757565298
NM_207361.6(FREM2):c.7519+16T>C
NM_207361.6(FREM2):c.7520-10_7520-9insCT rs1399473815
NM_207361.6(FREM2):c.7520-16_7520-15insG rs1555272871
NM_207361.6(FREM2):c.7520-16_7520-15insGT rs1555272871
NM_207361.6(FREM2):c.7520-5del rs36084034
NM_207361.6(FREM2):c.7520-5dup rs36084034
NM_207361.6(FREM2):c.7520-6_7520-5dup rs36084034
NM_207361.6(FREM2):c.7520-7_7520-5dup
NM_207361.6(FREM2):c.7983+16A>T
NM_207361.6(FREM2):c.7984-11del
NM_207361.6(FREM2):c.8281+23_8281+25del
NM_207361.6(FREM2):c.9006+12del
NM_207361.6(FREM2):c.9357G>C (p.Thr3119=) rs41306664

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