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: rs1057519966
rs1057519966
3 0.882 0.080 17 49619064 missense variant A/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1057519972
rs1057519972
3 0.882 0.080 17 49619327 missense variant A/T snv 0.010 1.000 1 2017 2017
dbSNP: rs1057520005
rs1057520005
14 0.742 0.360 17 7673800 missense variant C/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs1058808
rs1058808
27 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 1.000 1 2017 2017
dbSNP: rs1060501201
rs1060501201
4 0.925 0.080 17 7674190 missense variant T/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs10740051
rs10740051
2 0.925 0.080 10 46025670 intron variant C/T snv 0.24 0.010 1.000 1 2011 2011
dbSNP: rs10749408
rs10749408
2 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 0.010 1.000 1 2011 2011
dbSNP: rs10759932
rs10759932
15 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 0.010 1.000 1 2007 2007
dbSNP: rs1076064
rs1076064
4 0.851 0.160 5 149732603 intron variant A/G snv 0.47 0.010 1.000 1 2019 2019
dbSNP: rs10761581
rs10761581
2 0.925 0.080 10 46027444 missense variant A/C snv 0.44 0.41 0.010 1.000 1 2011 2011
dbSNP: rs10773338
rs10773338
2 0.925 0.080 12 126919857 intron variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs10788165
rs10788165
2 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs10895304
rs10895304
2 0.925 0.080 11 102519261 downstream gene variant A/G snv 0.20 0.010 1.000 1 2011 2011
dbSNP: rs10899221
rs10899221
2 0.925 0.080 11 76470587 intron variant G/A;T snv 5.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs10920531
rs10920531
2 0.925 0.080 1 202939708 downstream gene variant A/C snv 0.57 0.010 1.000 1 2016 2016
dbSNP: rs10973794
rs10973794
2 0.925 0.080 9 38409359 intron variant G/A snv 0.15 0.010 1.000 1 2017 2017
dbSNP: rs10987883
rs10987883
2 0.925 0.080 9 128118550 non coding transcript exon variant G/A snv 0.82 0.010 1.000 1 2011 2011
dbSNP: rs11063118
rs11063118
2 0.925 0.080 12 4372398 intron variant T/C;G snv 0.010 1.000 1 2014 2014
dbSNP: rs11067228
rs11067228
3 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 0.010 1.000 1 2013 2013
dbSNP: rs11079344
rs11079344
2 0.925 0.080 17 58297122 downstream gene variant A/G snv 0.14 0.010 1.000 1 2011 2011
dbSNP: rs11096955
rs11096955
5 0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 0.010 1.000 1 2008 2008
dbSNP: rs11096957
rs11096957
8 0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41 0.010 1.000 1 2008 2008
dbSNP: rs11102001
rs11102001
4 0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 0.010 1.000 1 2009 2009
dbSNP: rs11133373
rs11133373
4 0.851 0.120 4 55349464 intron variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs11168314
rs11168314
VDR
2 0.925 0.080 12 47936846 intron variant G/A snv 0.23 0.010 1.000 1 2010 2010