rs121913386, CDKN2A

N. diseases: 7
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 7 1996 2011
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 1 2014 2014
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 1.000 1 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 0