Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2012 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2012 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 < 0.001 1 2019 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C2242595
Disease: Mucosal atrophy
Mucosal atrophy 		0.010 < 0.001 1 2019 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0333983
Disease: Hyperplastic Polyp
Hyperplastic Polyp 		0.010 1.000 1 2019 2019
dbSNP: rs13428812
rs13428812
DNMT3A
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0238339
Disease: Hereditary pancreatitis
Hereditary pancreatitis 		0.010 1.000 1 2019 2019