rs2424913, DNMT3B

N. diseases: 18
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.030 1.000 3 2011 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.030 1.000 3 2011 2015
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.020 1.000 2 2015 2018
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.020 1.000 2 2015 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.020 1.000 2 2017 2017
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2011 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2016 2016
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2014 2014
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2009 2009
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2014 2014
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2013 2013
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2012 2012
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
98 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2017 2017
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2013 2013
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2017 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 0.010 1.000 1 2012 2012