Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2013 2015
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2013 2015
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 < 0.001 1 2019 2019
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0040100
Disease: Thymoma
Thymoma 		0.010 1.000 1 2013 2013
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome 		0.010 1.000 1 2015 2015
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0747845
Disease: early pregnancy
early pregnancy 		0.010 1.000 1 2017 2017
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.010 1.000 1 2013 2013
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 < 0.001 1 2019 2019
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.010 1.000 1 2015 2015
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 < 0.001 1 2019 2019
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2014 2014
dbSNP: rs1569686
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016