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.
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2012 2012
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2012 2012
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2008 2008
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1 2010 2010
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2012 2012
Malignant Glioma
CUI: C0555198
Disease: Malignant Glioma
22 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2012 2012
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1 2010 2010
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2010 2010
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2007 2007
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2019 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2018 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2010 2010
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005