rs11879293, SMARCA4

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.120 19 10961934 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.120 19 10961934 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.120 19 10961934 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.882 0.120 19 10961934 intron variant G/A;C;T snv 0.010 1.000 1 2014 2014