Source: ALL
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: rs116548533
rs116548533
CYP24A1
4 0.851 0.280 20 54159083 missense variant C/A;T snv 4.0E-06; 4.2E-04 0.010 1.000 1 2017 2017
dbSNP: rs121909796
rs121909796
VDR
5 0.827 0.200 12 47846743 missense variant C/A snv 0.010 1.000 1 2017 2017
dbSNP: rs121909800
rs121909800
VDR
6 0.807 0.360 12 47844859 missense variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs139280106
rs139280106
RELB
4 0.851 0.280 19 45032712 missense variant C/G;T snv 5.9E-05 0.010 1.000 1 2006 2006
dbSNP: rs377423996
rs377423996
VDR
4 0.851 0.280 12 47845002 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017
dbSNP: rs780229030
rs780229030
RELB
4 0.851 0.280 19 45032710 missense variant A/C snv 0.010 1.000 1 2006 2006