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: rs781933660
rs781933660
1 1.000 0.080 X 150657977 missense variant G/A snv 0.810 1.000 18 1997 2015
dbSNP: rs132630304
rs132630304
3 0.882 0.080 X 150598660 missense variant C/G;T snv 0.810 1.000 2 2012 2013
dbSNP: rs587783772
rs587783772
14 0.776 0.200 X 150659665 missense variant G/A;T snv 0.800 1.000 17 1997 2013
dbSNP: rs587783754
rs587783754
1 1.000 0.080 X 150657887 missense variant C/G snv 0.800 1.000 15 1997 2013
dbSNP: rs587783755
rs587783755
1 1.000 0.080 X 150657899 missense variant G/A snv 0.800 1.000 15 1997 2013
dbSNP: rs587783759
rs587783759
1 1.000 0.080 X 150657927 missense variant C/A snv 0.800 1.000 15 1997 2013
dbSNP: rs587783762
rs587783762
1 1.000 0.080 X 150657972 missense variant G/C snv 0.800 1.000 15 1997 2013
dbSNP: rs587783764
rs587783764
1 1.000 0.080 X 150658000 missense variant G/T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783796
rs587783796
1 1.000 0.080 X 150598600 missense variant G/A;T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783801
rs587783801
1 1.000 0.080 X 150663460 missense variant T/C snv 0.800 1.000 15 1997 2013
dbSNP: rs587783809
rs587783809
1 1.000 0.080 X 150598663 missense variant C/T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783816
rs587783816
1 1.000 0.080 X 150614617 missense variant T/C snv 0.800 1.000 15 1997 2013
dbSNP: rs587783832
rs587783832
1 1.000 0.080 X 150641275 missense variant C/T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783835
rs587783835
1 1.000 0.080 X 150641290 missense variant A/G snv 0.800 1.000 15 1997 2013
dbSNP: rs587783836
rs587783836
1 1.000 0.080 X 150641297 missense variant C/T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783841
rs587783841
1 1.000 0.080 X 150641354 missense variant C/T snv 0.800 1.000 15 1997 2013
dbSNP: rs587783848
rs587783848
1 1.000 0.080 X 150641416 missense variant C/A snv 0.800 1.000 15 1997 2013
dbSNP: rs587783850
rs587783850
1 1.000 0.080 X 150645683 missense variant G/A snv 0.800 1.000 15 1997 2013
dbSNP: rs587783851
rs587783851
1 1.000 0.080 X 150645687 missense variant T/C snv 0.800 1.000 15 1997 2013
dbSNP: rs587783856
rs587783856
1 1.000 0.080 X 150645795 missense variant T/G snv 0.800 1.000 15 1997 2013
dbSNP: rs132630302
rs132630302
1 1.000 0.080 X 150641306 missense variant A/G snv 0.800 1.000 1 2012 2012
dbSNP: rs132630303
rs132630303
1 1.000 0.080 X 150657957 missense variant A/G snv 0.800 1.000 1 2012 2012
dbSNP: rs132630305
rs132630305
1 1.000 0.080 X 150645725 missense variant C/T snv 0.800 1.000 1 2012 2012
dbSNP: rs132630307
rs132630307
1 1.000 0.080 X 150638967 missense variant G/A snv 0.800 1.000 1 2012 2012
dbSNP: rs886044782
rs886044782
1 1.000 0.080 X 150659694 missense variant G/A snv 0.700 1.000 14 1997 2013