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 0.020 1.000 2 2007 2016
dbSNP: rs1978124
rs1978124
2 X 15599940 intron variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs2074192
rs2074192
9 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2012 2012
dbSNP: rs2285666
rs2285666
4 0.925 0.160 X 15592225 splice region variant C/T snv 6.2E-06; 0.28 0.23 0.010 1.000 1 2018 2018
dbSNP: rs4240157
rs4240157
4 0.925 0.080 X 15568841 intron variant C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs4646188
rs4646188
4 0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 0.010 1.000 1 2012 2012