Source: ALL

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: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.710 1.000 2 2012 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.700 0
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 1997 2019
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2010 2019
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2004 2004
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.010 1.000 1 2004 2004
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney
0.010 1.000 1 2007 2007
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2004 2004
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 1995 1995
dbSNP: rs886039484
rs886039484
0.641 0.440 17 7674888 missense variant T/C;G snv
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma
0.010 1.000 1 2004 2004