rs1569686, DNMT3B

N. diseases: 15
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 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.020 1.000 2 2013 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.020 1.000 2 2013 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2016 2016
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2016 2016
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
early pregnancy
CUI: C0747845
Disease: early pregnancy
8 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2016 2016
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1 2019 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1 2019 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2016 2016
Thymoma
CUI: C0040100
Disease: Thymoma
20 0.752 0.400 20 32779273 intron variant G/A;C;T snv 0.010 1.000 1 2013 2013