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: rs1468271
rs1468271
2 1.000 0.040 7 24287362 intron variant C/T snv 0.97 0.020 1.000 2 2008 2009
dbSNP: rs11932595
rs11932595
12 0.827 0.160 4 55457430 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs17222772
rs17222772
3 0.925 0.120 13 30737959 intron variant A/T snv 0.010 1.000 1 2017 2017
dbSNP: rs17321515
rs17321515
16 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2009 2009
dbSNP: rs1746661
rs1746661
3 0.925 0.080 1 32869438 intron variant G/A;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1984112
rs1984112
8 0.807 0.280 7 80613604 intron variant A/G snv 0.33 0.010 1.000 1 2013 2013
dbSNP: rs2234693
rs2234693
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
dbSNP: rs2235543
rs2235543
4 0.925 0.080 1 209687323 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs3761740
rs3761740
4 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 0.010 1.000 1 2013 2013
dbSNP: rs4072032
rs4072032
2 1.000 0.040 17 64378896 intron variant G/A snv 0.40 0.010 1.000 1 2008 2008
dbSNP: rs4149081
rs4149081
5 1.000 0.040 12 21225087 intron variant G/A snv 0.18 0.010 1.000 1 2012 2012
dbSNP: rs4393158
rs4393158
2 1.000 0.040 1 209678552 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs4580704
rs4580704
13 0.790 0.200 4 55460540 intron variant G/C snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs4823613
rs4823613
1 1.000 0.040 22 46202410 intron variant A/G snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs6066394
rs6066394
2 1.000 0.040 20 47581409 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs6782181
rs6782181
6 0.851 0.160 3 138386212 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs804280
rs804280
6 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs515135
rs515135
9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.010 < 0.001 1 2019 2019
dbSNP: rs7566605
rs7566605
11 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 0.010 1.000 1 2009 2009
dbSNP: rs138947766
rs138947766
6 0.851 0.080 19 11116883 stop gained G/A;C snv 8.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs2228671
rs2228671
14 0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs879254509
rs879254509
3 0.882 0.080 19 11105295 stop gained C/G snv 0.010 1.000 1 2012 2012
dbSNP: rs879254597
rs879254597
4 0.851 0.120 19 11105528 stop gained G/A;T snv 0.010 1.000 1 2004 2004
dbSNP: rs144172724
rs144172724
6 0.851 0.080 19 11102774 stop gained G/A;T snv 1.6E-05 0.700 0