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: rs11543848
rs11543848
EGFR
0.790 0.240 7 55161562 missense variant G/A;C;T snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs2227983
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs373129709
rs373129709
EGFR ; LOC105375284
0.827 0.120 7 55019338 missense variant G/A;T snv 1.1E-04
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2007 2007
dbSNP: rs712829
rs712829
EGFR ; LOC105375284
0.776 0.120 7 55019062 5 prime UTR variant G/C;T snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019