rs6713088, ACYP2

N. diseases: 9
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.
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2017 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2016 2016
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2016 2016
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
55 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2019 2019
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2017 2017
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.763 0.200 2 54118332 intron variant C/G snv 0.48 0.010 1.000 1 2017 2017