ClinVar Miner

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

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_000426.3(LAMA2):c.2037G>C (p.Ala679=) rs398123369
NM_000426.3(LAMA2):c.3279C>T (p.Cys1093=) rs371376404
NM_000426.3(LAMA2):c.3861C>T (p.Ile1287=) rs138702650
NM_000426.3(LAMA2):c.6269-820A>G rs544696321
NM_000426.3(LAMA2):c.6269-829A>G rs758519410
NM_000426.3(LAMA2):c.6269-831C>G rs371162111
NM_000426.3(LAMA2):c.6269-831C>T rs371162111
NM_000426.3(LAMA2):c.6269-845C>T rs1554297888
NM_000426.3(LAMA2):c.6269-848T>A rs1554297884
NM_000426.3(LAMA2):c.6269-848T>C rs1554297884
NM_000426.3(LAMA2):c.6269-849C>T rs1554297881
NM_000426.3(LAMA2):c.6269-852A>C rs766496312
NM_000426.3(LAMA2):c.6269-855A>C rs1554297879
NM_000426.3(LAMA2):c.6269-855A>G rs1554297879
NM_000426.3(LAMA2):c.6269-855A>T rs1554297879
NM_000426.3(LAMA2):c.6269-856C>G rs763589558
NM_000426.3(LAMA2):c.6702A>T (p.Ala2234=) rs372212378
NM_000426.3(LAMA2):c.6786G>A (p.Ser2262=) rs398123382
NM_000426.3(LAMA2):c.7473A>G (p.Lys2491=) rs886038295
NM_000426.3(LAMA2):c.8907C>T (p.Arg2969=) rs367622610

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