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.
Costello syndrome (disorder)
CUI: C0587248
Disease: Costello syndrome (disorder)
19 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.830 1.000 17 1990 2017
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES
10 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.800 4 2005 2008
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
223 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.710 1.000 2 2012 2016
Genetic Diseases, Inborn
CUI: C0950123
Disease: Genetic Diseases, Inborn
827 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 9 2002 2018
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
35 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 5 2007 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 2 2015 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
180 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
223 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
203 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
53 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
389 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2015 2015
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
98 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
183 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
72 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
29 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
149 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Papillary renal cell carcinoma, sporadic
30 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
121 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Transitional cell carcinoma of bladder
147 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.615 0.464 11 534288 missense variant C/A,G,T snp 0.700 1 2016 2016