rs10433937, HSD17B13

N. diseases: 4
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.
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.882 0.080 4 87308948 intron variant T/A;C;G snv 0.010 1 2019 2019
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.882 0.080 4 87308948 intron variant T/A;C;G snv 0.010 1 2019 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.882 0.080 4 87308948 intron variant T/A;C;G snv 0.010 1 2019 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.882 0.080 4 87308948 intron variant T/A;C;G snv 0.010 1 2019 2019