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: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.030 0.667 3 2011 2017
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2008 2019
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 0.500 2 2017 2018
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
dbSNP: rs11574143
rs11574143
VDR
5 0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 0.010 1.000 1 2009 2009
dbSNP: rs2107301
rs2107301
VDR
7 0.807 0.120 12 47861787 intron variant G/A snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs2238135
rs2238135
VDR
4 0.882 0.160 12 47884407 intron variant C/G snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs2239182
rs2239182
VDR
2 0.925 0.080 12 47861628 intron variant T/C snv 0.51 0.010 1.000 1 2014 2014
dbSNP: rs2408876
rs2408876
VDR
2 0.925 0.080 12 47879782 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs7299460
rs7299460
VDR
2 0.925 0.080 12 47902485 intron variant C/T snv 0.43 0.010 1.000 1 2010 2010