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: rs121918350
rs121918350
1.000 0.120 20 10658612 missense variant G/A snv
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases 0.800 1.000 14 1997 2013