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 2017 2019
dbSNP: rs11168287
rs11168287
VDR
3 0.882 0.160 12 47891631 intron variant G/A snv 0.56 0.010 1.000 1 2016 2016
dbSNP: rs11574079
rs11574079
VDR
1 1.000 0.080 12 47858947 intron variant C/T snv 1.7E-03 0.010 1.000 1 2016 2016
dbSNP: rs11574143
rs11574143
VDR
5 0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 0.010 1.000 1 2016 2016
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 2019 2019
dbSNP: rs3819545
rs3819545
VDR
1 1.000 0.080 12 47871223 intron variant A/G snv 0.36 0.010 1.000 1 2016 2016
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 2019 2019
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2019 2019