rs13428812, DNMT3A

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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.800 1.000 1 2010 2010
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.020 1.000 2 2012 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.020 1.000 2 2012 2019
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1 2019 2019
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
Mucosal atrophy
CUI: C2242595
Disease: Mucosal atrophy
5 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.827 0.120 2 25269598 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019