ClinVar Miner

List of variants in gene LAMA2 reported as benign by Athena Diagnostics Inc

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_000426.3(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1586G>A (p.Ser529Asn) rs370691060
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.2430A>C (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6274+4C>T rs73775410
NM_000426.3(LAMA2):c.6429+8C>A rs199773264
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843
NM_000426.3(LAMA2):c.7760T>C (p.Val2587Ala) rs2229848
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.8028T>C (p.Asn2676=) rs35313209
NM_000426.3(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293
NM_000426.3(LAMA2):c.8548-10T>C rs113644365

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