ClinVar Miner

List of variants in gene LAMA2 reported as likely benign by PreventionGenetics

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Total variants: 42
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HGVS dbSNP
NM_000426.3(LAMA2):c.1206+11C>T rs115007959
NM_000426.3(LAMA2):c.1207-28G>A rs112735359
NM_000426.3(LAMA2):c.1467+38C>T rs78299321
NM_000426.3(LAMA2):c.1491T>C (p.Cys497=) rs2306220
NM_000426.3(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923
NM_000426.3(LAMA2):c.1782+14T>C rs191215452
NM_000426.3(LAMA2):c.1884+50A>C rs116773503
NM_000426.3(LAMA2):c.1930C>G (p.His644Asp) rs35879899
NM_000426.3(LAMA2):c.2376C>T (p.Phe792=) rs150046431
NM_000426.3(LAMA2):c.2476C>T (p.Arg826Trp) rs118147866
NM_000426.3(LAMA2):c.2736G>A (p.Ala912=) rs142671449
NM_000426.3(LAMA2):c.2749+24C>A rs886038292
NM_000426.3(LAMA2):c.2756G>T (p.Arg919Leu) rs35277491
NM_000426.3(LAMA2):c.2857-14T>A rs535718824
NM_000426.3(LAMA2):c.2857-39T>C rs117096733
NM_000426.3(LAMA2):c.3175-22G>A rs777129293
NM_000426.3(LAMA2):c.3556-15T>G rs17741922
NM_000426.3(LAMA2):c.3597T>C (p.Asp1199=) rs199904029
NM_000426.3(LAMA2):c.3969T>C (p.Thr1323=) rs112327654
NM_000426.3(LAMA2):c.4311+32C>G rs148912474
NM_000426.3(LAMA2):c.4718-37G>A rs115237621
NM_000426.3(LAMA2):c.5121C>T (p.Asp1707=) rs151199929
NM_000426.3(LAMA2):c.5280G>A (p.Glu1760=) rs376693904
NM_000426.3(LAMA2):c.5727-27C>A rs116128872
NM_000426.3(LAMA2):c.5769A>G (p.Ala1923=) rs200582139
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6649G>A (p.Val2217Ile) rs147857398
NM_000426.3(LAMA2):c.6702A>T (p.Ala2234=) rs372212378
NM_000426.3(LAMA2):c.6706A>C (p.Arg2236=) rs886038293
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7451+37A>G rs886038294
NM_000426.3(LAMA2):c.7452-9A>G rs748647936
NM_000426.3(LAMA2):c.7473A>G (p.Lys2491=) rs886038295
NM_000426.3(LAMA2):c.7573-9T>C rs369082375
NM_000426.3(LAMA2):c.8076-24A>G rs886038296
NM_000426.3(LAMA2):c.8548-10T>C rs113644365
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8907C>T (p.Arg2969=) rs367622610
NM_000426.3(LAMA2):c.8989-12C>G rs144860334
NM_000426.3(LAMA2):c.909+32T>A rs374692035
NM_000426.3(LAMA2):c.9211+21C>A rs886038297
NM_000426.3(LAMA2):c.9211+6T>C rs201375881

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