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: rs12931878
rs12931878
1 1.000 0.120 16 10948337 intron variant A/G snv 0.14 0.700 1.000 1 2007 2007
dbSNP: rs12923849
rs12923849
1 1.000 0.120 16 10968140 intron variant G/A snv 0.13 0.700 1.000 1 2007 2007
dbSNP: rs17229044
rs17229044
2 1.000 0.120 16 10969079 intron variant C/T snv 0.16 0.700 1.000 1 2007 2007
dbSNP: rs13330041
rs13330041
2 1.000 0.120 16 10994951 intron variant G/A snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs713041
rs713041
16 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 0.030 1.000 3 2013 2019
dbSNP: rs725613
rs725613
4 0.851 0.240 16 11075826 intron variant T/G snv 0.42 0.740 1.000 4 2007 2013
dbSNP: rs2041670
rs2041670
4 0.851 0.280 16 11080795 intron variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs7200786
rs7200786
3 0.882 0.200 16 11083944 intron variant A/G snv 0.59 0.700 1.000 1 2007 2007
dbSNP: rs4849135
rs4849135
1 1.000 0.120 2 110857502 intron variant T/G snv 0.67 0.700 1.000 1 2015 2015
dbSNP: rs12708716
rs12708716
7 0.807 0.320 16 11086016 intron variant A/G snv 0.37 0.800 1.000 5 2007 2011
dbSNP: rs886125
rs886125
1 1.000 0.120 12 110927520 intergenic variant A/G snv 0.57 0.700 1.000 1 2008 2008
dbSNP: rs12924729
rs12924729
3 0.882 0.200 16 11093926 intron variant G/A snv 0.34 0.700 1.000 1 2007 2007
dbSNP: rs12917716
rs12917716
4 0.851 0.200 16 11095291 intron variant G/C snv 0.51 0.010 1.000 1 2010 2010
dbSNP: rs12599402
rs12599402
2 0.925 0.160 16 11096031 intron variant T/C snv 0.51 0.700 1.000 1 2007 2007
dbSNP: rs12927355
rs12927355
3 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 0.800 1.000 2 2011 2015
dbSNP: rs998592
rs998592
2 0.925 0.160 16 11105821 intron variant C/T snv 0.39 0.700 1.000 1 2007 2007
dbSNP: rs9933507
rs9933507
1 1.000 0.120 16 11107571 intron variant T/C snv 0.46 0.700 1.000 1 2007 2007
dbSNP: rs1265564
rs1265564
4 1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 0.810 1.000 1 2012 2012
dbSNP: rs3184504
rs3184504
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.820 1.000 6 2009 2018
dbSNP: rs2903692
rs2903692
6 0.807 0.360 16 11144926 intron variant G/A snv 0.33 0.840 1.000 4 2007 2010
dbSNP: rs17673553
rs17673553
2 1.000 0.120 16 11148049 intron variant A/G snv 0.18 0.710 1.000 1 2007 2007
dbSNP: rs6498169
rs6498169
6 0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 0.020 1.000 2 2009 2010
dbSNP: rs653178
rs653178
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.710 1.000 2 2011 2015
dbSNP: rs2234702
rs2234702
1 1.000 0.120 11 111912374 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs17696736
rs17696736
18 0.827 0.240 12 112049014 intron variant A/G snv 0.30 0.810 1.000 4 2007 2010