rs7560488, None

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.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.851 0.160 2 25345952 upstream gene variant T/C snv 0.40 0.020 1.000 2 2014 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.851 0.160 2 25345952 upstream gene variant T/C snv 0.40 0.020 1.000 2 2014 2016
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.851 0.160 2 25345952 upstream gene variant T/C snv 0.40 0.010 1.000 1 2016 2016
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.851 0.160 2 25345952 upstream gene variant T/C snv 0.40 0.010 1.000 1 2015 2015