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: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs121913385
rs121913385
0.763 0.240 9 21971112 missense variant G/A;C snv
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm
0.700 0