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: rs3805490
rs3805490
0.925 0.080 5 40792051 intron variant T/A snv 0.21
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2018 2018
dbSNP: rs3805490
rs3805490
0.925 0.080 5 40792051 intron variant T/A snv 0.21
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2018 2018