rs10127775, GALNT2

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.
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2019 2019
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2012 2012
High density lipoprotein measurement
1440 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2019 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1 230160042 intron variant A/G;T snv 0.700 1.000 1 2019 2019