ClinVar Miner

List of variants in gene combination CHRM2, LOC349160 reported as uncertain significance for Cardiomyopathy

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001006630.2(CHRM2):c.1189A>G (p.Ile397Val) rs745902607 0.00004

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