rs183606230, CDH2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.882 0.080 18 28013691 missense variant A/G snv 4.0E-06 2.1E-05 0.010 1.000 1 2018 2018
Intrahepatic Cholangiocarcinoma
CUI: C0345905
Disease: Intrahepatic Cholangiocarcinoma
19 0.882 0.080 18 28013691 missense variant A/G snv 4.0E-06 2.1E-05 0.010 1.000 1 2018 2018
Primary cholangiocarcinoma of intrahepatic biliary tract
CUI: C4284013
Disease: Primary cholangiocarcinoma of intrahepatic biliary tract
10 0.882 0.080 18 28013691 missense variant A/G snv 4.0E-06 2.1E-05 0.010 1.000 1 2018 2018