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: rs35041767
rs35041767
1 1.000 0.080 9 9261737 intron variant -/C ins 0.700 1.000 1 2008 2008
dbSNP: rs1820989
rs1820989
1 1.000 0.080 2 67842758 intergenic variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs1836229
rs1836229
1 1.000 0.080 9 8820573 intron variant A/C;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2228570
rs2228570
VDR
99 0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 0.010 1.000 1 2015 2015
dbSNP: rs2280673
rs2280673
3 0.882 0.160 3 133839310 intron variant A/C;T snv 0.020 1.000 2 2016 2019
dbSNP: rs3810651
rs3810651
4 0.925 0.080 X 152652814 missense variant A/C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs6904723
rs6904723
1 1.000 0.080 6 38468541 intron variant A/C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs3923809
rs3923809
1 1.000 0.080 6 38473194 intron variant A/G snv 0.32 0.820 1.000 4 2007 2017
dbSNP: rs12593813
rs12593813
2 1.000 0.080 15 67744514 intron variant A/G snv 0.53 0.810 1.000 3 2007 2018
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.030 1.000 3 2015 2019
dbSNP: rs11635424
rs11635424
1 1.000 0.080 15 67745240 intron variant A/G snv 0.53 0.710 1.000 2 2007 2018
dbSNP: rs10208712
rs10208712
1 1.000 0.080 2 3986856 regulatory region variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs1052553
rs1052553
8 0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 0.010 1.000 1 2013 2013
dbSNP: rs12469063
rs12469063
2 0.925 0.080 2 66537176 intron variant A/G snv 0.18 0.700 1.000 1 2007 2007
dbSNP: rs17636328
rs17636328
1 1.000 0.080 6 37522755 intron variant A/G snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs1801260
rs1801260
28 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs35987657
rs35987657
1 1.000 0.080 3 130816723 upstream gene variant A/G snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs365032
rs365032
1 1.000 0.080 20 64164052 intron variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs6747972
rs6747972
1 1.000 0.080 2 67843093 intergenic variant A/G snv 0.65 0.810 1.000 1 2011 2011
dbSNP: rs7881785
rs7881785
1 1.000 0.080 X 42995357 upstream gene variant A/G snv 0.700 1.000 1 2007 2007
dbSNP: rs1830084
rs1830084
4 0.882 0.160 3 133789620 3 prime UTR variant A/G;T snv 0.020 1.000 2 2016 2019
dbSNP: rs855791
rs855791
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.020 1.000 2 2016 2019
dbSNP: rs10952927
rs10952927
1 1.000 0.080 7 88729746 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2071746
rs2071746
18 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.020 1.000 2 2015 2018
dbSNP: rs1848460
rs1848460
1 1.000 0.080 3 3406460 intron variant A/T snv 0.33 0.700 1.000 1 2017 2017