ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance for Inborn genetic diseases

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Total variants: 2
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599
NM_000744.6(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243

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