Source: BEFREE

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: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2013 2013
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2014 2014
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2017 2017
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2019 2019
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2015 2015
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis 		0.010 1.000 1 2020 2020
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		0.010 1.000 1 2020 2020
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2014 2014
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2018 2018
dbSNP: rs2228612
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2014 2014