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: rs11569142
rs11569142
EGF
1 4 110010783 intron variant G/T snv 1.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs377602035
rs377602035
EGF
1 4 109937360 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT delins 0.700 1.000 1 2016 2016