rs7136259, ATP2B1

N. diseases: 2
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 12 89687411 intron variant T/A;C;G snv 0.800 1.000 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 12 89687411 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019