rs2076211, PNPLA3

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.
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 1.000 22 43933198 intron variant C/A;T snv 0.18 0.700 1.000 1 2013 2013
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 22 43933198 intron variant C/A;T snv 0.18 0.700 1.000 1 2017 2017
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 1.000 22 43933198 intron variant C/A;T snv 0.18 0.700 1.000 1 2019 2019