ClinVar Miner

List of variants in gene LAMA2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Total variants: 103
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HGVS dbSNP
NM_000426.3(LAMA2):c.*207_*210dupATTT rs886061059
NM_000426.3(LAMA2):c.*46T>C rs376934472
NM_000426.3(LAMA2):c.-103C>T rs886061036
NM_000426.3(LAMA2):c.-89_-87delGCT rs568369254
NM_000426.3(LAMA2):c.-99A>G rs111531732
NM_000426.3(LAMA2):c.1084A>T (p.Arg362Ter)
NM_000426.3(LAMA2):c.1085G>T (p.Arg362Ile) rs182958473
NM_000426.3(LAMA2):c.112+3dupA rs886061040
NM_000426.3(LAMA2):c.1169G>C (p.Cys390Ser) rs886061045
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1373G>A (p.Arg458Lys) rs140604077
NM_000426.3(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726
NM_000426.3(LAMA2):c.1467+12A>G rs200224891
NM_000426.3(LAMA2):c.1467+1G>A rs1554234161
NM_000426.3(LAMA2):c.1506C>A (p.Ser502=) rs560445624
NM_000426.3(LAMA2):c.1550A>T (p.Glu517Val) rs372358704
NM_000426.3(LAMA2):c.1558T>C (p.Cys520Arg) rs886061046
NM_000426.3(LAMA2):c.1701C>T (p.Ile567=) rs111381107
NM_000426.3(LAMA2):c.1715C>T (p.Ala572Val) rs149811988
NM_000426.3(LAMA2):c.1716G>C (p.Ala572=) rs758682648
NM_000426.3(LAMA2):c.1782+10C>T rs200030296
NM_000426.3(LAMA2):c.1930C>G (p.His644Asp) rs35879899
NM_000426.3(LAMA2):c.194T>C (p.Met65Thr) rs886061041
NM_000426.3(LAMA2):c.2097-3T>C rs886061047
NM_000426.3(LAMA2):c.2115T>G (p.Leu705=) rs149753273
NM_000426.3(LAMA2):c.2149A>G (p.Ile717Val) rs369049149
NM_000426.3(LAMA2):c.2323-7T>G rs762740616
NM_000426.3(LAMA2):c.237G>A (p.Arg79=) rs201402165
NM_000426.3(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866
NM_000426.3(LAMA2):c.2527C>T (p.Arg843Cys) rs769493998
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2686C>T (p.Arg896Trp) rs764053957
NM_000426.3(LAMA2):c.2714A>G (p.Tyr905Cys) rs886061048
NM_000426.3(LAMA2):c.2736G>A (p.Ala912=) rs142671449
NM_000426.3(LAMA2):c.2857-13C>T rs201188972
NM_000426.3(LAMA2):c.3086G>A (p.Arg1029Gln) rs149993931
NM_000426.3(LAMA2):c.30T>G (p.Leu10=) rs886061038
NM_000426.3(LAMA2):c.3296A>G (p.Asn1099Ser) rs35065563
NM_000426.3(LAMA2):c.3304C>T (p.Arg1102Cys) rs755313913
NM_000426.3(LAMA2):c.3429C>A (p.Ile1143=) rs200646230
NM_000426.3(LAMA2):c.3555+10G>A rs767221324
NM_000426.3(LAMA2):c.3556-15T>G rs17741922
NM_000426.3(LAMA2):c.3666C>A (p.Asp1222Glu) rs373992160
NM_000426.3(LAMA2):c.3750G>T (p.Gly1250=) rs754604600
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4205G>A (p.Arg1402His) rs144830879
NM_000426.3(LAMA2):c.4222C>G (p.Arg1408Gly) rs780127363
NM_000426.3(LAMA2):c.463G>T (p.Glu155Ter)
NM_000426.3(LAMA2):c.4697G>A (p.Arg1566His) rs574923739
NM_000426.3(LAMA2):c.4790A>T (p.Asn1597Ile) rs566008145
NM_000426.3(LAMA2):c.4935C>A (p.Thr1645=) rs35579821
NM_000426.3(LAMA2):c.4944C>T (p.Asn1648=) rs111632017
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4993G>A (p.Gly1665Arg) rs373997222
NM_000426.3(LAMA2):c.5072-3C>A rs759155854
NM_000426.3(LAMA2):c.5179G>C (p.Glu1727Gln) rs374201203
NM_000426.3(LAMA2):c.5360G>C (p.Trp1787Ser) rs747621078
NM_000426.3(LAMA2):c.5446-14A>T rs886061049
NM_000426.3(LAMA2):c.5469C>T (p.Ser1823=) rs753886576
NM_000426.3(LAMA2):c.5558T>G (p.Ile1853Arg) rs141911213
NM_000426.3(LAMA2):c.5560G>A (p.Asp1854Asn) rs886061050
NM_000426.3(LAMA2):c.5665A>G (p.Lys1889Glu) rs886061051
NM_000426.3(LAMA2):c.5688C>T (p.His1896=) rs573779258
NM_000426.3(LAMA2):c.5893G>A (p.Glu1965Lys) rs886061052
NM_000426.3(LAMA2):c.6128A>G (p.Gln2043Arg) rs144155507
NM_000426.3(LAMA2):c.6133A>G (p.Asn2045Asp) rs886061053
NM_000426.3(LAMA2):c.61C>G (p.Gln21Glu) rs886061039
NM_000426.3(LAMA2):c.6206A>G (p.Tyr2069Cys) rs117884199
NM_000426.3(LAMA2):c.6268+5G>C rs182064878
NM_000426.3(LAMA2):c.6410C>T (p.Ala2137Val) rs886061054
NM_000426.3(LAMA2):c.6429+10T>G rs770063449
NM_000426.3(LAMA2):c.6438A>G (p.Val2146=) rs755485519
NM_000426.3(LAMA2):c.6563G>A (p.Ser2188Asn) rs372592018
NM_000426.3(LAMA2):c.6667A>G (p.Thr2223Ala) rs886061055
NM_000426.3(LAMA2):c.6739G>C (p.Ala2247Pro) rs750585696
NM_000426.3(LAMA2):c.6788C>T (p.Thr2263Met) rs56209257
NM_000426.3(LAMA2):c.6832A>G (p.Met2278Val) rs146854942
NM_000426.3(LAMA2):c.7057C>T (p.Arg2353Cys) rs145885540
NM_000426.3(LAMA2):c.7344T>C (p.Asn2448=) rs199931560
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7466T>C (p.Leu2489Pro) rs774287164
NM_000426.3(LAMA2):c.7479C>T (p.Ser2493=) rs368989339
NM_000426.3(LAMA2):c.7640G>A (p.Gly2547Glu) rs115488979
NM_000426.3(LAMA2):c.7708A>G (p.Thr2570Ala) rs144901086
NM_000426.3(LAMA2):c.7762A>G (p.Ile2588Val) rs886061056
NM_000426.3(LAMA2):c.7888C>T (p.Arg2630Ter) rs727502851
NM_000426.3(LAMA2):c.805A>G (p.Ile269Val) rs886061042
NM_000426.3(LAMA2):c.818G>A (p.Arg273Lys) rs886061043
NM_000426.3(LAMA2):c.819+7T>C rs886061044
NM_000426.3(LAMA2):c.8223G>A (p.Thr2741=) rs150596964
NM_000426.3(LAMA2):c.8464T>C (p.Leu2822=) rs199570699
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8633T>G (p.Ile2878Ser) rs886061057
NM_000426.3(LAMA2):c.8728G>A (p.Val2910Ile) rs141479751
NM_000426.3(LAMA2):c.8836G>A (p.Gly2946Arg) rs370843758
NM_000426.3(LAMA2):c.8982T>C (p.Asp2994=) rs79374915
NM_000426.3(LAMA2):c.8989-12C>G rs144860334
NM_000426.3(LAMA2):c.9123C>T (p.Val3041=) rs61749497
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599
NM_000426.3(LAMA2):c.9240C>A (p.Thr3080=) rs759819184
NM_000426.3(LAMA2):c.9328G>A (p.Glu3110Lys) rs140829166
NM_000426.3(LAMA2):c.98C>A (p.Ala33Glu) rs750280423
NM_000426.3:c.6820delG

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