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: rs10937275
rs10937275
1 1.000 0.071 3 186933001 intron variant A/G snp 0.88 0.800 1 2009 2009
dbSNP: rs1497546
rs1497546
1 1.000 0.071 3 98315682 intron variant G/A snp 8.6E-02 0.800 1 2009 2009
dbSNP: rs2395029
rs2395029
5 0.878 0.107 6 31464003 non coding transcript exon variant T/G snp 2.7E-02 2.2E-02 0.800 1 2009 2009
dbSNP: rs1050450
rs1050450
21 0.692 0.500 3 49357401 missense variant G/A snp 0.28 0.30 0.010 1.000 1 2010 2010
dbSNP: rs3129900
rs3129900
3 0.878 0.179 6 32338202 intron variant G/T snp 0.83 0.800 1 2010 2010
dbSNP: rs4880
rs4880
81 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 0.010 1.000 1 2010 2010
dbSNP: rs2523822
rs2523822
1 1.000 0.071 6 29860883 intergenic variant A/G snp 0.28 0.800 1 2011 2011
dbSNP: rs3135388
rs3135388
4 0.846 0.250 6 32445274 intergenic variant A/G snp 0.90 0.010 1.000 1 2011 2011
dbSNP: rs9274407
rs9274407
3 0.878 0.143 6 32665055 stop lost A/C,T snp 0.77 0.78 0.810 1.000 1 2011 2011
dbSNP: rs17036170
rs17036170
1 1.000 0.071 3 12288912 5 prime UTR variant G/A snp 1.4E-02 0.800 1 2013 2013
dbSNP: rs231775
rs231775
38 0.608 0.536 2 203867991 missense variant A/G,T snp 0.42; 4.0E-06 0.42 0.010 1.000 1 2013 2013
dbSNP: rs3087243
rs3087243
19 0.715 0.357 2 203874196 intergenic variant G/A snp 0.35 0.010 1.000 1 2013 2013
dbSNP: rs4553808
rs4553808
5 0.878 0.107 2 203866282 intergenic variant A/G snp 0.16 0.010 1.000 1 2013 2013
dbSNP: rs5742909
rs5742909
9 0.756 0.214 2 203867624 intergenic variant C/T snp 7.1E-02 0.010 1.000 1 2013 2013
dbSNP: rs733618
rs733618
1 1.000 0.071 2 203866221 intergenic variant T/C snp 0.11 0.010 1.000 1 2013 2013
dbSNP: rs7574865
rs7574865
36 0.618 0.571 2 191099907 intron variant T/G snp 0.79 0.010 1.000 1 2013 2013
dbSNP: rs138642043
rs138642043
1 1.000 0.071 2 168964291 missense variant C/T snp 3.4E-03 5.5E-03 0.010 1.000 1 2014 2014
dbSNP: rs2287622
rs2287622
16 0.707 0.179 2 168973818 missense variant A/C,G,T snp 0.57 0.57 0.010 1.000 1 2014 2014
dbSNP: rs2741045
rs2741045
3 1.000 0.071 2 233671494 intron variant C/T snp 0.22 0.010 1.000 1 2016 2016
dbSNP: rs7828135
rs7828135
1 1.000 0.071 8 80146584 intron variant T/C snp 0.11 0.700 1 2016 2016
dbSNP: rs10404821
rs10404821
1 1.000 0.071 19 50657831 intron variant C/A,T snp 0.38 0.700 1 2017 2017
dbSNP: rs112655218
rs112655218
1 1.000 0.071 18 9841518 intron variant G/A snp 5.2E-02 0.700 1 2017 2017
dbSNP: rs113206698
rs113206698
1 1.000 0.071 10 92818147 intergenic variant G/A snp 3.1E-02 0.700 1 2017 2017
dbSNP: rs114577328
rs114577328
1 1.000 0.071 6 29959505 intron variant G/C snp 9.9E-03 0.700 1 2017 2017
dbSNP: rs114811931
rs114811931
1 1.000 0.071 5 161257724 intergenic variant T/C snp 2.3E-02 0.700 1 2017 2017