rs1057519883, CDKN2A

N. diseases: 14
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.
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Papillary renal cell carcinoma, sporadic
30 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
348 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 1.000 1 2016 2016
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
25 0.742 0.280 9 21971120 missense variant C/G;T snv 0.700 0
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.742 0.280 9 21971120 missense variant C/G;T snv 0.010 1.000 1 2018 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.742 0.280 9 21971120 missense variant C/G;T snv 0.010 1.000 1 2018 2018