ClinVar Miner

List of variants reported as uncertain significance for congenital urachal anomaly by CHLA Center for Personalized Medicine,Children's Hospital, Los Angeles

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_000379.4(XDH):c.1172C>T (p.Pro391Leu) rs1558697792
NM_000379.4(XDH):c.3647C>A (p.Pro1216His) rs143981573

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