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: rs1934179
rs1934179
2 0.925 0.120 X 50439186 intron variant G/A snv 0.46 0.720 1.000 2 2011 2015
dbSNP: rs4554617
rs4554617
2 0.925 0.120 X 50460404 intron variant A/C snv 0.45 0.710 1.000 2 2014 2019
dbSNP: rs11091748
rs11091748
2 0.925 0.120 X 50414986 intron variant A/G snv 0.39 0.010 1.000 1 2018 2018
dbSNP: rs12171755
rs12171755
2 0.925 0.120 X 50436751 intron variant C/T snv 0.30 0.010 1.000 1 2018 2018
dbSNP: rs1934190
rs1934190
2 0.925 0.120 X 50400967 intron variant G/A;C snv 0.33 0.010 1.000 1 2015 2015
dbSNP: rs2211122
rs2211122
2 0.925 0.120 X 50459752 intron variant T/C snv 0.45 0.010 1.000 1 2019 2019
dbSNP: rs4599945
rs4599945
2 0.925 0.120 X 50380968 intron variant G/A;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs4826632
rs4826632
2 0.925 0.120 X 50454263 intron variant G/T snv 0.46 0.010 < 0.001 1 2015 2015