ClinVar Miner

List of variants in gene LAMA2 reported as pathogenic by Counsyl

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Total variants: 16
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HGVS dbSNP
NM_000426.3(LAMA2):c.1122del (p.Gly376fs) rs1338860420
NM_000426.3(LAMA2):c.1303C>T (p.Arg435Ter) rs773209126
NM_000426.3(LAMA2):c.2230C>T (p.Arg744Ter) rs775676341
NM_000426.3(LAMA2):c.3085C>T (p.Arg1029Ter) rs145420388
NM_000426.3(LAMA2):c.363C>A (p.Tyr121Ter) rs535635043
NM_000426.3(LAMA2):c.3799_3821del (p.Phe1267fs) rs750220830
NM_000426.3(LAMA2):c.3976C>T (p.Arg1326Ter) rs398123373
NM_000426.3(LAMA2):c.4048C>T (p.Arg1350Ter) rs756854513
NM_000426.3(LAMA2):c.4645C>T (p.Arg1549Ter) rs121913575
NM_000426.3(LAMA2):c.5116C>T (p.Arg1706Ter) rs758775001
NM_000426.3(LAMA2):c.5156_5159del (p.Lys1719fs) rs1554286963
NM_000426.3(LAMA2):c.5476C>T (p.Arg1826Ter) rs747349942
NM_000426.3(LAMA2):c.7147C>T (p.Arg2383Ter) rs121913576
NM_000426.3(LAMA2):c.7490_7493dup (p.Asp2498fs) rs1480934961
NM_000426.3(LAMA2):c.7732C>T (p.Arg2578Ter) rs121913572
NM_000426.3(LAMA2):c.8244+1G>A rs749522728

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