rs1550117, DNMT3A

N. diseases: 11
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 neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.020 1.000 2 2015 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.020 1.000 2 2015 2016
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2016 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2016 2016
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2016 2016
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2013 2013
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2013 2013
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2015 2015
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 0.010 1.000 1 2015 2015