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: rs114619974
rs114619974 		1.000 0.080 4 105234376 missense variant G/A snv 5.2E-04 2.2E-03
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs116519313
rs116519313 		1.000 0.080 4 105276128 missense variant T/C;G snv 1.3E-05
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1283441077
rs1283441077 		1.000 0.080 4 105276331 missense variant C/T snv 6.4E-06
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1316795626
rs1316795626 		1.000 0.080 4 105276287 missense variant G/A snv 6.4E-06
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1406914931
rs1406914931 		1.000 0.080 4 105276431 missense variant G/T snv
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs376570662
rs376570662 		1.000 0.080 4 105235321 missense variant C/T snv 1.2E-04 1.7E-04
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs532738858
rs532738858 		1.000 0.080 4 105236763 missense variant C/T snv 1.2E-05 2.1E-05
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs569067880
rs569067880 		0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs569067880
rs569067880 		0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 0
dbSNP: rs749210253
rs749210253 		1.000 0.080 4 105272630 missense variant G/A;T snv 3.8E-05; 6.4E-06
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs754215085
rs754215085 		1.000 0.080 4 105276407 missense variant G/A snv 5.7E-05 1.4E-05
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs767475870
rs767475870 		1.000 0.040 4 105276203 missense variant C/T snv
CUI: C0280449
Disease: secondary acute myeloid leukemia
secondary acute myeloid leukemia 		Neoplasms 0.700 0
dbSNP: rs771761785
rs771761785 		1.000 0.080 4 105243757 missense variant G/A;C snv 6.4E-06
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.700 0
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: 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
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
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
CUI: C0346629
Disease: Malignant neoplasm of large intestine
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
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019