rs2612091, ENOSF1

N. diseases: 3
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.
Hyalinosis, Systemic
CUI: C2745948
Disease: Hyalinosis, Systemic
30 0.882 0.160 18 683607 intron variant C/T snv 0.63 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.882 0.160 18 683607 intron variant C/T snv 0.63 0.010 1.000 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.882 0.160 18 683607 intron variant C/T snv 0.63 0.010 1.000 1 2017 2017