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: rs28935476
rs28935476
1 X 53432110 missense variant G/C snv 5.5E-06 9.5E-06 0.810 1.000 1 2019 2019
dbSNP: rs122461163
rs122461163
1 X 53431450 missense variant T/C snv 0.800 1.000 12 2003 2017
dbSNP: rs587777651
rs587777651
1 X 53432347 missense variant T/C snv 0.800 1.000 12 2003 2017
dbSNP: rs62626305
rs62626305
1 X 53431445 missense variant C/G snv 0.800 1.000 12 2003 2017
dbSNP: rs28935475
rs28935475
1 X 53432086 missense variant G/A snv 0.800 0
dbSNP: rs886041974
rs886041974
1 X 53431556 missense variant T/C snv 0.800 0
dbSNP: rs104886492
rs104886492
3 1.000 0.120 X 53432410 missense variant A/G snv 0.700 1.000 12 2003 2017
dbSNP: rs122462164
rs122462164
1 X 53431819 splice region variant G/T snv 0.700 0
dbSNP: rs1556894502
rs1556894502
1 X 53431513 missense variant C/T snv 0.700 0
dbSNP: rs886037927
rs886037927
1 X 53431801 missense variant G/T snv 0.700 0