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: rs6479891
rs6479891
1 1.000 0.120 10 63246696 intron variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs10761744
rs10761744
1 1.000 0.120 10 63341266 intron variant C/G;T snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs10761745
rs10761745
3 0.882 0.240 10 63341311 intron variant G/C snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs2893922
rs2893922
1 1.000 0.120 10 63487259 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs7082090
rs7082090
1 1.000 0.120 10 63239252 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs9414780
rs9414780
1 1.000 0.120 10 63241673 intron variant A/C snv 0.87 0.700 1.000 1 2012 2012
dbSNP: rs9414788
rs9414788
1 1.000 0.120 10 63296952 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9415699
rs9415699
1 1.000 0.120 10 63383798 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9415705
rs9415705
1 1.000 0.120 10 63401790 intron variant T/G snv 0.13 0.700 1.000 1 2012 2012