TET2, tet methylcytosine dioxygenase 2, 54790

N. diseases: 362; N. variants: 47
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4698934
rs4698934
1.000 0.040 4 105218230 intron variant T/C snv 0.12
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.810 1.000 1 2014 2014
dbSNP: rs9790517
rs9790517
0.925 0.080 4 105163621 intron variant C/T snv 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.710 1.000 4 2013 2017
dbSNP: rs9790517
rs9790517
0.925 0.080 4 105163621 intron variant C/T snv 0.20
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.710 1.000 2 2013 2015
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs11726786
rs11726786
4 105199599 intron variant T/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2019
dbSNP: rs1391438
rs1391438
4 105230686 intron variant T/C snv 0.71
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2018
dbSNP: rs2047409
rs2047409
1.000 0.040 4 105215876 intron variant G/A snv 0.49
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.700 1.000 2 2017 2019
dbSNP: rs2647249
rs2647249
4 105264506 intron variant C/T snv 0.82
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2018
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2010 2010
dbSNP: rs10010325
rs10010325
1.000 0.040 4 105185196 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs10022109
rs10022109
4 105166665 intron variant A/G snv 0.20
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs1391440
rs1391440
4 105195804 intron variant C/G snv 0.50
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs1391441
rs1391441
0.763 0.240 4 105207603 intron variant G/A snv 0.70
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs139887111
rs139887111
4 105195057 intron variant -/T delins 0.31
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs143875052
rs143875052
4 105229398 intron variant C/T snv 0.11
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019