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: rs12924729
rs12924729
3 0.882 0.200 16 11093926 intron variant G/A snv 0.34 0.800 1.000 3 2011 2015
dbSNP: rs12708715
rs12708715
1 1.000 0.080 16 11083967 intron variant C/T snv 0.39 0.800 1.000 1 2012 2012
dbSNP: rs12935413
rs12935413
3 1.000 0.080 16 11116590 intron variant G/A snv 0.34 0.700 1.000 2 2011 2012
dbSNP: rs12708716
rs12708716
7 0.807 0.320 16 11086016 intron variant A/G snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs12925642
rs12925642
1 1.000 0.080 16 11077745 intron variant A/G snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs12927355
rs12927355
3 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs2041670
rs2041670
4 0.851 0.280 16 11080795 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2058531
rs2058531
1 1.000 0.080 16 11078252 intron variant T/C snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs7203793
rs7203793
1 1.000 0.080 16 11088277 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs725613
rs725613
4 0.851 0.240 16 11075826 intron variant T/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs9652582
rs9652582
1 1.000 0.080 16 11080707 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs9746695
rs9746695
1 1.000 0.080 16 11114037 intron variant T/A;C snv 0.32 0.700 1.000 1 2012 2012