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: rs1143630
rs1143630
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2019 2019
dbSNP: rs1143630
rs1143630
0.827 0.160 2 112834078 intron variant T/A;G snv
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2012 2012
dbSNP: rs1143630
rs1143630
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2019 2019
dbSNP: rs1143630
rs1143630
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1143630
rs1143630
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2011 2011