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: rs2073043
rs2073043
1 X 150473747 missense variant A/G snv 0.11 0.10 0.010 1.000 1 2012 2012
dbSNP: rs41313406
rs41313406
1 X 150470648 missense variant C/T snv 8.3E-02 8.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs62641609
rs62641609
1 X 150470614 missense variant C/A snv 5.4E-03 1.9E-02 0.010 1.000 1 2012 2012