rs6733868, DNMT3A

N. diseases: 6
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.
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.851 0.120 2 25276998 intron variant C/G snv 0.50 0.010 1.000 1 2019 2019