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: rs11209026
rs11209026
24 0.673 0.321 1 67240275 missense variant G/A snp 4.2E-02 4.5E-02 0.900 0.800 12 2008 2016
dbSNP: rs20541
rs20541
29 0.638 0.607 5 132660272 missense variant A/G snp 0.72 0.75 0.860 0.833 10 2008 2016
dbSNP: rs610604
rs610604
5 0.821 0.214 6 137878280 intron variant G/T snp 0.59 0.860 0.833 10 2009 2016
dbSNP: rs12191877
rs12191877
3 0.878 0.071 6 31285148 intron variant C/T snp 0.12 0.830 1.000 5 2009 2016
dbSNP: rs2201841
rs2201841
10 0.744 0.357 1 67228519 intron variant A/G,T snp 0.28 0.830 1.000 5 2009 2016
dbSNP: rs33980500
rs33980500
9 0.784 0.071 6 111592059 missense variant C/T snp 8.6E-02 9.1E-02 0.830 1.000 5 2010 2014
dbSNP: rs17728338
rs17728338
4 0.846 0.143 5 151098757 regulatory region variant G/A snp 7.3E-02 0.820 1.000 7 2009 2016
dbSNP: rs4795067
rs4795067
1 1.000 0.036 17 27779649 intron variant A/G snp 0.31 0.820 1.000 5 2010 2016
dbSNP: rs4112788
rs4112788
4 0.846 0.107 1 152578800 intergenic variant A/G,T snp 0.67 0.820 1.000 4 2009 2011
dbSNP: rs11652075
rs11652075
2 0.923 0.036 17 80205094 missense variant C/T snp 0.41 0.41 0.820 1.000 3 2012 2013
dbSNP: rs2066808
rs2066808
5 0.846 0.214 12 56344189 intron variant A/G snp 0.20 0.810 1.000 5 2009 2015
dbSNP: rs495337
rs495337
2 0.923 0.107 20 49905793 synonymous variant G/A snp 0.44 0.36 0.810 1.000 4 2008 2015
dbSNP: rs8016947
rs8016947
2 0.923 0.071 14 35363460 intron variant T/G snp 0.58 0.810 1.000 4 2010 2016
dbSNP: rs27524
rs27524
3 0.878 0.143 5 96766240 intron variant A/G snp 0.62 0.810 1.000 3 2010 2015
dbSNP: rs2395029
rs2395029
5 0.878 0.107 6 31464003 non coding transcript exon variant T/G snp 2.7E-02 2.2E-02 0.810 1.000 2 2008 2015
dbSNP: rs4649203
rs4649203
3 0.878 0.071 1 24193430 intergenic variant G/A snp 0.61 0.810 1.000 2 2010 2014
dbSNP: rs10484554
rs10484554
5 0.846 0.107 6 31306778 intron variant C/T snp 0.12 0.800 3 2008 2016
dbSNP: rs11795343
rs11795343
1 1.000 0.036 9 32523739 intron variant T/C snp 0.40 0.800 3 2013 2016
dbSNP: rs12720356
rs12720356
10 0.769 0.214 19 10359299 missense variant A/C,G snp 6.1E-02; 4.0E-06 6.2E-02 0.800 3 2010 2017
dbSNP: rs17716942
rs17716942
2 0.923 0.036 2 162404181 intron variant T/C snp 8.9E-02 0.800 3 2010 2015
dbSNP: rs240993
rs240993
1 1.000 0.036 6 111352511 intron variant T/A,C snp 0.54 0.800 3 2010 2016
dbSNP: rs582757
rs582757
6 0.801 0.143 6 137876687 intron variant C/T snp 0.70 0.800 3 2013 2017
dbSNP: rs10782001
rs10782001
3 1.000 0.036 16 30931304 intron variant G/A snp 0.55 0.800 2 2010 2015
dbSNP: rs12188300
rs12188300
6 0.801 0.107 5 159402519 A/G,T snp 5.5E-02 0.800 2 2013 2017
dbSNP: rs12586317
rs12586317
1 1.000 0.036 14 35212966 intron variant T/C snp 0.21 0.800 2 2010 2015