ClinVar Miner

List of variants in gene CDKN1C studied for Beckwith-Wiedemann syndrome; Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies

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Total variants: 2
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NM_000076.2(CDKN1C):c.-266G>A rs147317732
NM_001122630.2(CDKN1C):c.815C>T (p.Ala272Val) rs776541692

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