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: rs121913675
rs121913675
0.925 0.080 7 116778953 missense variant C/T snv
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs121913676
rs121913676
0.925 0.080 7 116783421 missense variant G/A;C;T snv
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs121913677
rs121913677
0.925 0.080 7 116783402 missense variant A/G snv
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma
Digestive System Diseases; Neoplasms 0.700 0