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: rs117913411
rs117913411
VDR
1 12 47860570 intron variant T/A snv 3.2E-02 0.700 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 2019 2019
dbSNP: rs2189480
rs2189480
VDR
2 1.000 0.040 12 47870045 intron variant G/T snv 0.36 0.010 1.000 1 2019 2019
dbSNP: rs2239179
rs2239179
VDR
9 0.790 0.200 12 47863983 intron variant T/C snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs2248098
rs2248098
VDR
4 0.925 0.120 12 47859573 intron variant A/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs3847987
rs3847987
VDR
4 0.882 0.160 12 47844285 3 prime UTR variant C/A snv 0.12 0.010 1.000 1 2019 2019