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.
melanoma
CUI: C0025202
Disease: melanoma
389 0.769 0.143 4 54727495 missense variant T/C snp 0.750 1.000 16 1995 2015
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
90 0.769 0.143 4 54727495 missense variant T/C snp 0.730 1.000 4 2006 2017
Thymoma
CUI: C0040100
Disease: Thymoma
17 0.769 0.143 4 54727495 missense variant T/C snp 0.700 3 2007 2012
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.769 0.143 4 54727495 missense variant T/C snp 0.700 1 2007 2007
Thymic Carcinoma
CUI: C0205969
Disease: Thymic Carcinoma
5 0.769 0.143 4 54727495 missense variant T/C snp 0.010 1.000 1 2009 2009
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
20 0.769 0.143 4 54727495 missense variant T/C snp 0.010 1.000 1 2010 2010
Thymoma, type C
CUI: C1322286
Disease: Thymoma, type C
4 0.769 0.143 4 54727495 missense variant T/C snp 0.010 1.000 1 2009 2009
Esophageal Stenosis
CUI: C0014866
Disease: Esophageal Stenosis
1 0.769 0.143 4 54727495 missense variant T/C snp 0.010 1.000 1 2013 2013
Malignant melanoma, metastatic
CUI: C0860594
Disease: Malignant melanoma, metastatic
4 0.769 0.143 4 54727495 missense variant T/C snp 0.010 1.000 1 2005 2005