ClinVar Miner

List of variants reported as likely pathogenic for Hyperinsulinism due to HNF4A deficiency

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Total variants: 2
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HGVS dbSNP
NM_000457.4(HNF4A):c.1010_1012TGC[6] (p.Leu341dup) rs776489992
NM_000457.4(HNF4A):c.266G>A (p.Arg89Gln) rs1555813319

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