Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11568972
rs11568972
EGF
1 4 109967851 intron variant A/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs1860129
rs1860129
EGF
1 4 109965187 intron variant G/C snv 0.55 0.700 1.000 1 2018 2018