ClinVar Miner

List of variants reported as risk factor for Coronary artery disease, susceptibility to

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000446.7(PON1):c.575A>G (p.Gln192Arg)	rs662	0.42215
NM_000446.7(PON1):c.163T>A (p.Leu55Met)	rs854560	0.29107
NM_005544.3(IRS1):c.2911G>A (p.Gly971Arg)	rs1801278	0.06031

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