Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 7 1996 2011
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2014 2014
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
0.700 1.000 1 2016 2016
dbSNP: rs121913386
rs121913386
0.807 0.120 9 21971018 missense variant G/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.700 0