Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3774968
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs3774968
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs3774968
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.010 1.000 1 2013 2013
dbSNP: rs3774968
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2014 2014