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: rs1474348
rs1474348
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1474348
rs1474348
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2017 2017
dbSNP: rs1474348
rs1474348
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2017 2017
dbSNP: rs1474348
rs1474348
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2017 2017