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: rs2106809
rs2106809
8 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.040 1.000 4 2014 2019
dbSNP: rs4646155
rs4646155
3 0.925 0.080 X 15579386 intron variant C/T snv 3.9E-02 0.030 1.000 3 2018 2019
dbSNP: rs879922
rs879922
4 0.882 0.160 X 15572684 intron variant C/G snv 0.030 1.000 3 2018 2019
dbSNP: rs2074192
rs2074192
9 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.020 1.000 2 2018 2019
dbSNP: rs4240157
rs4240157
4 0.925 0.080 X 15568841 intron variant C/T snv 0.020 1.000 2 2018 2019
dbSNP: rs4646188
rs4646188
4 0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 0.020 1.000 2 2018 2019
dbSNP: rs4830542
rs4830542
3 0.925 0.080 X 15558483 downstream gene variant C/G;T snv 0.020 1.000 2 2018 2019
dbSNP: rs2048683
rs2048683
1 1.000 0.040 X 15590376 intron variant T/G snv 0.010 < 0.001 1 2018 2018
dbSNP: rs6632677
rs6632677
4 0.851 0.120 X 15596749 intron variant G/C snv 5.0E-03 0.010 < 0.001 1 2018 2018