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: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2010 2010
dbSNP: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1408543226
rs1408543226
XPA
0.807 0.240 9 97675558 missense variant A/G snv 7.0E-06
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.010 1.000 1 2006 2006