Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1554201713
rs1554201713
1.000 0.040 5 177267592 missense variant C/G snv
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.700 0