rs505922, ABO

N. diseases: 34
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.
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2018 2018
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2012 2012
Iron deficiency
CUI: C0240066
Disease: Iron deficiency
13 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1 2012 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2012 2012
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015