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: rs3807992
rs3807992
0.925 0.080 7 116557191 intron variant G/A snv 0.28
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs3807992
rs3807992
0.925 0.080 7 116557191 intron variant G/A snv 0.28
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.010 1.000 1 2013 2013
dbSNP: rs3807992
rs3807992
0.925 0.080 7 116557191 intron variant G/A snv 0.28
CUI: C0872084
Disease: Sarcopenia
Sarcopenia
0.010 1.000 1 2015 2015
dbSNP: rs3807992
rs3807992
0.925 0.080 7 116557191 intron variant G/A snv 0.28
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs3807992
rs3807992
0.925 0.080 7 116557191 intron variant G/A snv 0.28
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013