rs10456100, KCNK5

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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 1.000 0.040 6 39215694 intron variant C/T snv 0.20 0.800 1.000 3 2013 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 6 39215694 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018