ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 123
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HGVS dbSNP gnomAD frequency
NM_000426.4(LAMA2):c.8977A>G (p.Ile2993Val) rs145331792 0.00036
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.4205G>A (p.Arg1402His) rs144830879 0.00024
NM_000426.4(LAMA2):c.5405G>T (p.Arg1802Leu) rs141235562 0.00022
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.4909G>A (p.Glu1637Lys) rs138303386 0.00019
NM_000426.4(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826 0.00014
NM_000426.4(LAMA2):c.9188C>A (p.Pro3063His) rs151285465 0.00014
NM_000426.4(LAMA2):c.9008A>G (p.Asn3003Ser) rs747619612 0.00013
NM_000426.4(LAMA2):c.623C>A (p.Pro208His) rs183890063 0.00010
NM_000426.4(LAMA2):c.4166T>C (p.Leu1389Pro) rs752934825 0.00009
NM_000426.4(LAMA2):c.2670A>C (p.Lys890Asn) rs201625640 0.00006
NM_000426.4(LAMA2):c.3662T>G (p.Met1221Arg) rs140895872 0.00006
NM_000426.4(LAMA2):c.3806C>T (p.Thr1269Ile) rs375051351 0.00006
NM_000426.4(LAMA2):c.4786A>G (p.Ile1596Val) rs774875437 0.00005
NM_000426.4(LAMA2):c.676G>A (p.Asp226Asn) rs149654569 0.00005
NM_000426.4(LAMA2):c.7681G>A (p.Gly2561Ser) rs200341138 0.00005
NM_000426.4(LAMA2):c.2512G>A (p.Gly838Arg) rs150361703 0.00004
NM_000426.4(LAMA2):c.2831A>G (p.Gln944Arg) rs141920360 0.00004
NM_000426.4(LAMA2):c.3133G>T (p.Ala1045Ser) rs373373855 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.7058G>A (p.Arg2353His) rs548483084 0.00004
NM_000426.4(LAMA2):c.7118C>T (p.Ser2373Leu) rs758887080 0.00004
NM_000426.4(LAMA2):c.2916T>G (p.Phe972Leu) rs763840955 0.00003
NM_000426.4(LAMA2):c.4646G>A (p.Arg1549Gln) rs778508100 0.00003
NM_000426.4(LAMA2):c.518A>T (p.Asp173Val) rs767671585 0.00003
NM_000426.4(LAMA2):c.5692G>T (p.Ala1898Ser) rs1231472133 0.00003
NM_000426.4(LAMA2):c.7899-3C>T rs549227397 0.00003
NM_000426.4(LAMA2):c.2039A>G (p.Asn680Ser) rs774139365 0.00002
NM_000426.4(LAMA2):c.5593C>T (p.Pro1865Ser) rs563638833 0.00002
NM_000426.4(LAMA2):c.6647G>A (p.Arg2216His) rs371191809 0.00002
NM_000426.4(LAMA2):c.8426A>G (p.Asn2809Ser) rs769892018 0.00002
NM_000426.4(LAMA2):c.848T>C (p.Val283Ala) rs376917587 0.00002
NM_000426.4(LAMA2):c.8821G>A (p.Gly2941Arg) rs748373493 0.00002
NM_000426.4(LAMA2):c.1364G>A (p.Arg455Gln) rs201177178 0.00001
NM_000426.4(LAMA2):c.1496G>A (p.Arg499His) rs752075358 0.00001
NM_000426.4(LAMA2):c.1705A>C (p.Ile569Leu) rs766909163 0.00001
NM_000426.4(LAMA2):c.2089A>G (p.Ile697Val) rs778059153 0.00001
NM_000426.4(LAMA2):c.2794A>G (p.Ser932Gly) rs761539740 0.00001
NM_000426.4(LAMA2):c.281A>G (p.Asn94Ser) rs758713214 0.00001
NM_000426.4(LAMA2):c.3035C>T (p.Thr1012Ile) rs752658943 0.00001
NM_000426.4(LAMA2):c.4123G>A (p.Asp1375Asn) rs146827694 0.00001
NM_000426.4(LAMA2):c.4665G>C (p.Arg1555Ser) rs768204363 0.00001
NM_000426.4(LAMA2):c.4699G>A (p.Glu1567Lys) rs371388948 0.00001
NM_000426.4(LAMA2):c.4882G>A (p.Ala1628Thr) rs1239378825 0.00001
NM_000426.4(LAMA2):c.5318G>A (p.Arg1773Gln) rs573287715 0.00001
NM_000426.4(LAMA2):c.5335T>C (p.Tyr1779His) rs746898932 0.00001
NM_000426.4(LAMA2):c.5518G>A (p.Asp1840Asn) rs759350875 0.00001
NM_000426.4(LAMA2):c.5536G>A (p.Ala1846Thr) rs764965268 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.6518A>G (p.Asn2173Ser) rs529110314 0.00001
NM_000426.4(LAMA2):c.680A>G (p.Asp227Gly) rs757635528 0.00001
NM_000426.4(LAMA2):c.8125C>T (p.Arg2709Cys) rs769324317 0.00001
NM_000426.4(LAMA2):c.8398G>A (p.Gly2800Ser) rs758491978 0.00001
NM_000426.4(LAMA2):c.98C>A (p.Ala33Glu) rs750280423 0.00001
NM_000426.4(LAMA2):c.1290G>C (p.Glu430Asp)
NM_000426.4(LAMA2):c.1304G>A (p.Arg435Gln)
NM_000426.4(LAMA2):c.1363C>T (p.Arg455Trp)
NM_000426.4(LAMA2):c.1460T>C (p.Ile487Thr)
NM_000426.4(LAMA2):c.1775G>A (p.Gly592Glu)
NM_000426.4(LAMA2):c.1783C>T (p.Leu595Phe)
NM_000426.4(LAMA2):c.2246T>C (p.Ile749Thr)
NM_000426.4(LAMA2):c.2539T>C (p.Cys847Arg)
NM_000426.4(LAMA2):c.2549G>T (p.Gly850Val)
NM_000426.4(LAMA2):c.2660T>G (p.Leu887Arg)
NM_000426.4(LAMA2):c.2687G>A (p.Arg896Gln)
NM_000426.4(LAMA2):c.2852G>A (p.Cys951Tyr)
NM_000426.4(LAMA2):c.2945G>A (p.Ser982Asn) rs755096239
NM_000426.4(LAMA2):c.2951A>G (p.Gln984Arg)
NM_000426.4(LAMA2):c.2968G>C (p.Gly990Arg)
NM_000426.4(LAMA2):c.3053A>G (p.His1018Arg)
NM_000426.4(LAMA2):c.3130T>C (p.Cys1044Arg) rs2114461161
NM_000426.4(LAMA2):c.3239A>G (p.Asn1080Ser)
NM_000426.4(LAMA2):c.3242G>A (p.Cys1081Tyr)
NM_000426.4(LAMA2):c.3242G>T (p.Cys1081Phe)
NM_000426.4(LAMA2):c.3284G>A (p.Arg1095Gln)
NM_000426.4(LAMA2):c.3500A>G (p.Tyr1167Cys)
NM_000426.4(LAMA2):c.3539G>C (p.Gly1180Ala) rs762434314
NM_000426.4(LAMA2):c.3694C>G (p.Pro1232Ala) rs201391981
NM_000426.4(LAMA2):c.4222C>G (p.Arg1408Gly) rs780127363
NM_000426.4(LAMA2):c.4290C>A (p.Asp1430Glu)
NM_000426.4(LAMA2):c.4598G>C (p.Gly1533Ala)
NM_000426.4(LAMA2):c.4721G>C (p.Cys1574Ser)
NM_000426.4(LAMA2):c.4823T>C (p.Met1608Thr)
NM_000426.4(LAMA2):c.5137A>C (p.Asn1713His)
NM_000426.4(LAMA2):c.5172G>T (p.Met1724Ile)
NM_000426.4(LAMA2):c.5284C>T (p.Arg1762Trp) rs746492572
NM_000426.4(LAMA2):c.5351A>C (p.Asp1784Ala)
NM_000426.4(LAMA2):c.5378C>T (p.Ala1793Val)
NM_000426.4(LAMA2):c.5512A>C (p.Ile1838Leu)
NM_000426.4(LAMA2):c.5765C>T (p.Thr1922Ile)
NM_000426.4(LAMA2):c.5937C>G (p.Asn1979Lys) rs747714599
NM_000426.4(LAMA2):c.6280G>A (p.Asp2094Asn)
NM_000426.4(LAMA2):c.652T>A (p.Leu218Ile)
NM_000426.4(LAMA2):c.6646C>T (p.Arg2216Cys)
NM_000426.4(LAMA2):c.6766G>T (p.Val2256Leu)
NM_000426.4(LAMA2):c.7051G>A (p.Val2351Ile)
NM_000426.4(LAMA2):c.7112T>G (p.Phe2371Cys) rs201274841
NM_000426.4(LAMA2):c.7190A>C (p.His2397Pro)
NM_000426.4(LAMA2):c.731G>A (p.Arg244Lys)
NM_000426.4(LAMA2):c.7631T>C (p.Ile2544Thr) rs769655658
NM_000426.4(LAMA2):c.7913A>T (p.Gln2638Leu) rs1200724538
NM_000426.4(LAMA2):c.7957C>G (p.Gln2653Glu)
NM_000426.4(LAMA2):c.7984G>A (p.Val2662Ile)
NM_000426.4(LAMA2):c.8018C>T (p.Pro2673Leu)
NM_000426.4(LAMA2):c.8156A>G (p.Glu2719Gly)
NM_000426.4(LAMA2):c.8243A>T (p.His2748Leu)
NM_000426.4(LAMA2):c.8399G>T (p.Gly2800Val) rs749056462
NM_000426.4(LAMA2):c.8419C>G (p.Arg2807Gly) rs754671210
NM_000426.4(LAMA2):c.8422A>G (p.Ile2808Val)
NM_000426.4(LAMA2):c.858G>A (p.Met286Ile)
NM_000426.4(LAMA2):c.8638G>A (p.Asp2880Asn)
NM_000426.4(LAMA2):c.8678A>C (p.Asn2893Thr)
NM_000426.4(LAMA2):c.8855C>G (p.Ala2952Gly)
NM_000426.4(LAMA2):c.9212-1G>A rs398123391
NM_000426.4(LAMA2):c.9252C>G (p.Phe3084Leu) rs763815272
NM_000426.4(LAMA2):c.928G>C (p.Glu310Gln)
NM_000426.4(LAMA2):c.9337G>T (p.Gly3113Cys)
NM_000426.4(LAMA2):c.941G>T (p.Cys314Phe)

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