Source: BEFREE

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: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2016 2016
dbSNP: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
Adult Hepatocellular Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.010 1.000 1 2016 2016
dbSNP: rs1760893
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2016 2016