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: rs3761548
rs3761548
42 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2019
dbSNP: rs3761549
rs3761549
18 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 0.020 1.000 2 2014 2019
dbSNP: rs3761547
rs3761547
3 0.882 0.200 X 49262004 intron variant T/C snv 9.6E-02 0.010 1.000 1 2014 2014