rs2228612, DNMT1

N. diseases: 12
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.
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2015 2015
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2014 2014
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2014 2014
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2018 2018
Generalized osteoarthritis
CUI: C1384584
Disease: Generalized osteoarthritis
10 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2020 2020
Idiopathic osteoarthritis
CUI: C0409952
Disease: Idiopathic osteoarthritis
12 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2020 2020
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2017 2017
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2013 2013
melanoma
CUI: C0025202
Disease: melanoma
515 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 0.010 1.000 1 2017 2017