ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance by GeneDx

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Total variants: 138
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209 0.00164
NM_000426.4(LAMA2):c.2382C>T (p.Gly794=) rs147744763 0.00070
NM_000426.4(LAMA2):c.946G>A (p.Asp316Asn) rs141340479 0.00067
NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698 0.00066
NM_000426.4(LAMA2):c.3154A>G (p.Ser1052Gly) rs149165006 0.00061
NM_000426.4(LAMA2):c.5531G>A (p.Arg1844His) rs150691000 0.00056
NM_000426.4(LAMA2):c.7250A>G (p.His2417Arg) rs147185142 0.00053
NM_000426.4(LAMA2):c.1645C>T (p.Pro549Ser) rs139070796 0.00052
NM_000426.4(LAMA2):c.3014A>G (p.Asn1005Ser) rs139244736 0.00052
NM_000426.4(LAMA2):c.6506A>G (p.Asn2169Ser) rs144845618 0.00051
NM_000426.4(LAMA2):c.2009G>A (p.Arg670His) rs149305108 0.00034
NM_000426.4(LAMA2):c.3244C>T (p.His1082Tyr) rs146490004 0.00028
NM_000426.4(LAMA2):c.6832A>G (p.Met2278Val) rs146854942 0.00026
NM_000426.4(LAMA2):c.4010A>G (p.His1337Arg) rs139739075 0.00024
NM_000426.4(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169 0.00023
NM_000426.4(LAMA2):c.8905C>T (p.Arg2969Cys) rs374888837 0.00021
NM_000426.4(LAMA2):c.8920A>T (p.Thr2974Ser) rs140202046 0.00021
NM_000426.4(LAMA2):c.2932G>A (p.Asp978Asn) rs202050052 0.00020
NM_000426.4(LAMA2):c.4909G>A (p.Glu1637Lys) rs138303386 0.00019
NM_000426.4(LAMA2):c.7415G>T (p.Gly2472Val) rs200921233 0.00019
NM_000426.4(LAMA2):c.4675G>A (p.Gly1559Ser) rs377630412 0.00016
NM_000426.4(LAMA2):c.7057C>T (p.Arg2353Cys) rs145885540 0.00016
NM_000426.4(LAMA2):c.4650T>A (p.Pro1550=) rs545186322 0.00015
NM_000426.4(LAMA2):c.1873A>G (p.Ile625Val) rs141658354 0.00014
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826 0.00014
NM_000426.4(LAMA2):c.9001G>C (p.Val3001Leu) rs189360899 0.00013
NM_000426.4(LAMA2):c.1816A>G (p.Ile606Val) rs113022759 0.00012
NM_000426.4(LAMA2):c.2132A>G (p.Tyr711Cys) rs201122410 0.00012
NM_000426.4(LAMA2):c.725G>A (p.Arg242His) rs373570586 0.00012
NM_000426.4(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077 0.00011
NM_000426.4(LAMA2):c.3004G>A (p.Gly1002Ser) rs200953311 0.00011
NM_000426.4(LAMA2):c.4462G>A (p.Gly1488Arg) rs200961385 0.00011
NM_000426.4(LAMA2):c.533C>T (p.Thr178Met) rs148665727 0.00011
NM_000426.4(LAMA2):c.8842G>A (p.Gly2948Ser) rs143638361 0.00011
NM_000426.4(LAMA2):c.2767G>A (p.Gly923Ser) rs144492513 0.00010
NM_000426.4(LAMA2):c.4060A>G (p.Ile1354Val) rs143674727 0.00010
NM_000426.4(LAMA2):c.623C>A (p.Pro208His) rs183890063 0.00010
NM_000426.4(LAMA2):c.8467C>T (p.Pro2823Ser) rs151334775 0.00010
NM_000426.4(LAMA2):c.4166T>C (p.Leu1389Pro) rs752934825 0.00009
NM_000426.4(LAMA2):c.715C>T (p.Arg239Cys) rs145465528 0.00009
NM_000426.4(LAMA2):c.6563G>A (p.Ser2188Asn) rs372592018 0.00008
NM_000426.4(LAMA2):c.6598C>T (p.Arg2200Cys) rs568648664 0.00007
NM_000426.4(LAMA2):c.2288C>T (p.Ala763Val) rs141521127 0.00006
NM_000426.4(LAMA2):c.437C>G (p.Ser146Cys) rs143680577 0.00006
NM_000426.4(LAMA2):c.6884G>A (p.Arg2295His) rs142164767 0.00006
NM_000426.4(LAMA2):c.7978C>A (p.Leu2660Ile) rs201587923 0.00006
NM_000426.4(LAMA2):c.9145C>G (p.Gln3049Glu) rs146525742 0.00006
NM_000426.4(LAMA2):c.1562C>T (p.Ser521Leu) rs369760070 0.00005
NM_000426.4(LAMA2):c.149C>T (p.Ala50Val) rs191899712 0.00004
NM_000426.4(LAMA2):c.2686C>T (p.Arg896Trp) rs764053957 0.00004
NM_000426.4(LAMA2):c.2831A>G (p.Gln944Arg) rs141920360 0.00004
NM_000426.4(LAMA2):c.4118C>T (p.Pro1373Leu) rs754163400 0.00004
NM_000426.4(LAMA2):c.4685A>G (p.His1562Arg) rs767903280 0.00004
NM_000426.4(LAMA2):c.5050G>A (p.Glu1684Lys) rs201632009 0.00004
NM_000426.4(LAMA2):c.521C>T (p.Thr174Met) rs752992990 0.00004
NM_000426.4(LAMA2):c.6047T>C (p.Leu2016Ser) rs773309064 0.00004
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461 0.00004
NM_000426.4(LAMA2):c.6875A>T (p.Asp2292Val) rs749043823 0.00004
NM_000426.4(LAMA2):c.8690G>A (p.Arg2897Gln) rs201696115 0.00004
NM_000426.4(LAMA2):c.1529A>G (p.Asp510Gly) rs772958683 0.00003
NM_000426.4(LAMA2):c.2477G>A (p.Arg826Gln) rs759973830 0.00003
NM_000426.4(LAMA2):c.4646G>A (p.Arg1549Gln) rs778508100 0.00003
NM_000426.4(LAMA2):c.4717+4C>T rs200898063 0.00003
NM_000426.4(LAMA2):c.4960-17C>A rs758048596 0.00003
NM_000426.4(LAMA2):c.518A>T (p.Asp173Val) rs767671585 0.00003
NM_000426.4(LAMA2):c.665G>C (p.Arg222Thr) rs1267371641 0.00003
NM_000426.4(LAMA2):c.8222C>T (p.Thr2741Met) rs766816598 0.00003
NM_000426.4(LAMA2):c.1495C>T (p.Arg499Cys) rs143626559 0.00002
NM_000426.4(LAMA2):c.3461G>T (p.Gly1154Val) rs922954882 0.00002
NM_000426.4(LAMA2):c.358G>A (p.Glu120Lys) rs778869610 0.00002
NM_000426.4(LAMA2):c.5984T>C (p.Leu1995Pro) rs983616957 0.00002
NM_000426.4(LAMA2):c.848T>C (p.Val283Ala) rs376917587 0.00002
NM_000426.4(LAMA2):c.908A>C (p.Asn303Thr) rs753228224 0.00002
NM_000426.4(LAMA2):c.1792G>A (p.Val598Ile) rs753232836 0.00001
NM_000426.4(LAMA2):c.2008C>T (p.Arg670Cys) rs1324159581 0.00001
NM_000426.4(LAMA2):c.2084A>T (p.Asp695Val) rs762272518 0.00001
NM_000426.4(LAMA2):c.2392A>G (p.Lys798Glu) rs755581747 0.00001
NM_000426.4(LAMA2):c.2897C>T (p.Pro966Leu) rs774276037 0.00001
NM_000426.4(LAMA2):c.3129A>T (p.Lys1043Asn) rs772541077 0.00001
NM_000426.4(LAMA2):c.335G>A (p.Ser112Asn) rs754373965 0.00001
NM_000426.4(LAMA2):c.4595A>G (p.Tyr1532Cys) rs763732088 0.00001
NM_000426.4(LAMA2):c.5318G>A (p.Arg1773Gln) rs573287715 0.00001
NM_000426.4(LAMA2):c.5404C>T (p.Arg1802Cys) rs761866721 0.00001
NM_000426.4(LAMA2):c.5978A>G (p.Asp1993Gly) rs752249871 0.00001
NM_000426.4(LAMA2):c.6323G>A (p.Arg2108Gln) rs750999777 0.00001
NM_000426.4(LAMA2):c.6500A>G (p.Tyr2167Cys) rs1042387625 0.00001
NM_000426.4(LAMA2):c.6708-8C>G rs1562581016 0.00001
NM_000426.4(LAMA2):c.7437G>C (p.Leu2479Phe) rs1353846096 0.00001
NM_000426.4(LAMA2):c.8076-7C>G rs555377928 0.00001
NM_000426.4(LAMA2):c.8759C>T (p.Ala2920Val) rs757583844 0.00001
NM_000426.4(LAMA2):c.9217C>T (p.Leu3073Phe) rs1315125567 0.00001
NM_000426.4(LAMA2):c.98C>A (p.Ala33Glu) rs750280423 0.00001
NM_000426.4(LAMA2):c.1127G>T (p.Gly376Val)
NM_000426.4(LAMA2):c.1235A>G (p.Gln412Arg) rs776412628
NM_000426.4(LAMA2):c.1558T>A (p.Cys520Ser) rs886061046
NM_000426.4(LAMA2):c.1609-41=
NM_000426.4(LAMA2):c.1670A>C (p.Gln557Pro) rs1333451961
NM_000426.4(LAMA2):c.1782+3_1782+6del rs1781610935
NM_000426.4(LAMA2):c.1916A>T (p.Asp639Val) rs2114287007
NM_000426.4(LAMA2):c.2054T>C (p.Leu685Pro) rs746641607
NM_000426.4(LAMA2):c.2227A>G (p.Arg743Gly) rs1787575888
NM_000426.4(LAMA2):c.2233G>A (p.Val745Ile)
NM_000426.4(LAMA2):c.2564C>G (p.Pro855Arg) rs754714449
NM_000426.4(LAMA2):c.2780C>T (p.Ser927Phe) rs1085307732
NM_000426.4(LAMA2):c.3292T>C (p.Trp1098Arg) rs2114494197
NM_000426.4(LAMA2):c.32T>C (p.Leu11Pro) rs730880252
NM_000426.4(LAMA2):c.3317G>A (p.Cys1106Tyr) rs371548755
NM_000426.4(LAMA2):c.3547C>T (p.Arg1183Trp) rs867302949
NM_000426.4(LAMA2):c.3555+5G>A rs2114499515
NM_000426.4(LAMA2):c.3694C>G (p.Pro1232Ala) rs201391981
NM_000426.4(LAMA2):c.3778G>A (p.Glu1260Lys) rs1363185527
NM_000426.4(LAMA2):c.3850G>C (p.Ala1284Pro) rs1085307846
NM_000426.4(LAMA2):c.3871A>G (p.Met1291Val) rs780806324
NM_000426.4(LAMA2):c.436_437delinsAA (p.Ser146Asn)
NM_000426.4(LAMA2):c.4657A>G (p.Thr1553Ala) rs1450772080
NM_000426.4(LAMA2):c.4745T>C (p.Leu1582Pro) rs1349013414
NM_000426.4(LAMA2):c.479A>G (p.Asp160Gly) rs147398243
NM_000426.4(LAMA2):c.4945G>C (p.Glu1649Gln) rs143215851
NM_000426.4(LAMA2):c.525G>C (p.Glu175Asp) rs1554217596
NM_000426.4(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.4(LAMA2):c.5598G>T (p.Met1866Ile) rs1554289926
NM_000426.4(LAMA2):c.5741C>G (p.Ala1914Gly) rs2114697609
NM_000426.4(LAMA2):c.5833G>A (p.Ala1945Thr) rs3828736
NM_000426.4(LAMA2):c.6070T>G (p.Ser2024Ala)
NM_000426.4(LAMA2):c.6274+5G>T rs367765202
NM_000426.4(LAMA2):c.670A>G (p.Ser224Gly) rs1085307718
NM_000426.4(LAMA2):c.6977A>G (p.Lys2326Arg) rs1783185621
NM_000426.4(LAMA2):c.6993-7_6993-3del rs1380376723
NM_000426.4(LAMA2):c.70C>G (p.Arg24Gly) rs868408509
NM_000426.4(LAMA2):c.7112T>G (p.Phe2371Cys) rs201274841
NM_000426.4(LAMA2):c.7139T>G (p.Leu2380Arg) rs758211853
NM_000426.4(LAMA2):c.7334A>T (p.Gln2445Leu)
NM_000426.4(LAMA2):c.7390G>T (p.Ala2464Ser) rs1131691621
NM_000426.4(LAMA2):c.7901T>A (p.Ile2634Asn) rs2114859477
NM_000426.4(LAMA2):c.8918C>T (p.Thr2973Met) rs145842163
NM_000426.4(LAMA2):c.898C>T (p.Pro300Ser) rs2114964188
NM_000426.4(LAMA2):c.917G>A (p.Arg306His) rs1023922833
NM_000426.4(LAMA2):c.9269_9283dup (p.Thr3094_Lys3095insThrLeuLysLeuThr) rs1554321191

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