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: rs2890658
rs2890658
0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs2890658
rs2890658
0.925 0.080 9 5465130 intron variant C/A;T snv
Squamous cell carcinoma of esophagus
0.010 1.000 1 2017 2017
dbSNP: rs2890658
rs2890658
0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs2890658
rs2890658
0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019