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: rs2074192
rs2074192
9 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs4240157
rs4240157
4 0.925 0.080 X 15568841 intron variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs4646155
rs4646155
3 0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 0.010 1.000 1 2019 2019
dbSNP: rs4830542
rs4830542
3 0.925 0.080 X 15558483 downstream gene variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs6632677
rs6632677
4 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 1.000 1 2017 2017