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: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2011 2016
dbSNP: rs10735810
rs10735810
VDR
26 0.662 0.640 12 47879112 start lost A/C;G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs11568820
rs11568820
VDR
27 0.672 0.480 12 47908762 intron variant C/T snv 0.38 0.010 1.000 1 2011 2011
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 2008 2008
dbSNP: rs2239186
rs2239186
VDR
5 0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 0.010 1.000 1 2016 2016
dbSNP: rs4516035
rs4516035
VDR
10 0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 0.010 1.000 1 2008 2008
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2011 2011
dbSNP: rs739837
rs739837
VDR
5 0.882 0.200 12 47844438 3 prime UTR variant G/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs7976091
rs7976091
VDR
2 1.000 0.040 12 47910769 intron variant C/T snv 0.38 0.010 1.000 1 2011 2011