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: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
Papillary renal cell carcinoma, sporadic
0.700 1.000 1 2016 2016
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
0.700 0
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2018 2018