ClinVar Miner

List of variants in gene LAMA2 reported as likely benign for Laminin alpha 2-related dystrophy

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Total variants: 57
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HGVS dbSNP
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923
NM_000426.3(LAMA2):c.1722C>G (p.Ala574=) rs777308198
NM_000426.3(LAMA2):c.219C>G (p.Val73=) rs767540192
NM_000426.3(LAMA2):c.2230C>A (p.Arg744=) rs775676341
NM_000426.3(LAMA2):c.2451-5C>T rs1484837428
NM_000426.3(LAMA2):c.255C>T (p.Ile85=) rs142083777
NM_000426.3(LAMA2):c.2755C>T (p.Arg919Cys) rs138018456
NM_000426.3(LAMA2):c.2766C>T (p.Ala922=) rs149254699
NM_000426.3(LAMA2):c.3279C>T (p.Cys1093=) rs371376404
NM_000426.3(LAMA2):c.3447G>A (p.Arg1149=) rs1554269500
NM_000426.3(LAMA2):c.3528T>G (p.Ser1176=) rs1462835620
NM_000426.3(LAMA2):c.4101A>G (p.Gly1367=) rs746835015
NM_000426.3(LAMA2):c.4176+9C>T rs117116822
NM_000426.3(LAMA2):c.4786A>G (p.Ile1596Val) rs774875437
NM_000426.3(LAMA2):c.4857A>G (p.Leu1619=) rs777158791
NM_000426.3(LAMA2):c.4896T>G (p.Leu1632=) rs1554282062
NM_000426.3(LAMA2):c.4926A>G (p.Thr1642=) rs62421010
NM_000426.3(LAMA2):c.4959+6G>T rs148060790
NM_000426.3(LAMA2):c.4971G>C (p.Val1657=) rs749664821
NM_000426.3(LAMA2):c.4993G>A (p.Gly1665Arg) rs373997222
NM_000426.3(LAMA2):c.5079T>C (p.Asn1693=) rs752400396
NM_000426.3(LAMA2):c.5509G>A (p.Asp1837Asn) rs749423866
NM_000426.3(LAMA2):c.5530C>T (p.Arg1844Cys) rs56173620
NM_000426.3(LAMA2):c.5689G>A (p.Ala1897Thr) rs200518204
NM_000426.3(LAMA2):c.5726+8A>G rs1554290006
NM_000426.3(LAMA2):c.5901C>G (p.Ala1967=) rs1554295233
NM_000426.3(LAMA2):c.5969-5C>T rs201853235
NM_000426.3(LAMA2):c.6002G>A (p.Arg2001Lys) rs151009169
NM_000426.3(LAMA2):c.612C>G (p.Ser204=) rs201236591
NM_000426.3(LAMA2):c.6206A>G (p.Tyr2069Cys) rs117884199
NM_000426.3(LAMA2):c.6350A>G (p.Lys2117Arg) rs750866614
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.6702A>T (p.Ala2234=) rs372212378
NM_000426.3(LAMA2):c.6708-3A>C rs112637707
NM_000426.3(LAMA2):c.7111T>G (p.Phe2371Val) rs150644209
NM_000426.3(LAMA2):c.7155+9del rs781778543
NM_000426.3(LAMA2):c.7300+10T>A rs200469923
NM_000426.3(LAMA2):c.7301-9C>T rs747783456
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7425G>A (p.Thr2475=) rs1445712042
NM_000426.3(LAMA2):c.7440-9G>A rs369558532
NM_000426.3(LAMA2):c.7584A>C (p.Thr2528=) rs757763024
NM_000426.3(LAMA2):c.7640G>A (p.Gly2547Glu) rs115488979
NM_000426.3(LAMA2):c.7772A>G (p.Asn2591Ser) rs200095274
NM_000426.3(LAMA2):c.8181A>C (p.Ile2727=) rs1483437741
NM_000426.3(LAMA2):c.8223G>A (p.Thr2741=) rs150596964
NM_000426.3(LAMA2):c.8282T>C (p.Ile2761Thr) rs115650537
NM_000426.3(LAMA2):c.8298C>T (p.Phe2766=) rs145295628
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8692A>C (p.Arg2898=) rs200718262
NM_000426.3(LAMA2):c.8727C>T (p.Cys2909=) rs148285711
NM_000426.3(LAMA2):c.8728G>A (p.Val2910Ile) rs141479751
NM_000426.3(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295
NM_000426.3(LAMA2):c.8858-10C>T rs900145350
NM_000426.3(LAMA2):c.9211+6T>C rs201375881
NM_000426.3(LAMA2):c.945C>T (p.Gly315=) rs764217699

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