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: rs1801689
rs1801689
1 17 66214462 missense variant A/C,G snp 4.0E-06; 2.4E-02; 4.8E-05 1.9E-02 0.800 3 2012 2014
dbSNP: rs8017377
rs8017377
1 14 24414681 missense variant G/A snp 0.37 0.34 0.800 3 2010 2017
dbSNP: rs2328223
rs2328223
1 20 17865277 intergenic variant A/C,G,T snp 0.19 0.800 2 2014 2017
dbSNP: rs267733
rs267733
1 1 150986360 missense variant A/G snp 0.12 0.12 0.800 2 2014 2017
dbSNP: rs2710642
rs2710642
1 2 62922422 intron variant G/A snp 0.72 0.800 2 2014 2017
dbSNP: rs364585
rs364585
1 20 12982070 intergenic variant A/G snp 0.69 0.800 2 2014 2017
dbSNP: rs4942486
rs4942486
1 13 32379251 intron variant T/C snp 0.53 0.800 2 2014 2017
dbSNP: rs5763662
rs5763662
1 22 29982714 non coding transcript exon variant C/T snp 3.1E-02 0.800 2 2014 2017
dbSNP: rs1006725
rs1006725
1 10 112970444 intron variant A/G snp 6.5E-03 0.700 1 2012 2012
dbSNP: rs10087178
rs10087178
1 8 10111284 intron variant T/C snp 6.1E-02 0.700 1 2012 2012
dbSNP: rs10212320
rs10212320
1 3 30632373 intron variant C/T snp 7.1E-03 0.700 1 2012 2012
dbSNP: rs10306121
rs10306121
1 9 122372369 intron variant A/T snp 6.1E-02 0.700 1 2012 2012
dbSNP: rs10433493
rs10433493
1 3 190647811 intron variant G/C snp 1.9E-02 0.700 1 2012 2012
dbSNP: rs10495399
rs10495399
1 1 237648783 intron variant T/G snp 5.4E-02 0.700 1 2012 2012
dbSNP: rs11075663
rs11075663
1 16 67935887 intron variant T/G snp 3.6E-02 0.700 1 2012 2012
dbSNP: rs11192141
rs11192141
1 10 82005843 intron variant G/A snp 2.9E-02 0.700 1 2012 2012
dbSNP: rs1144302
rs1144302
F3
1 1 94534558 intron variant C/T snp 3.8E-02 0.700 1 2012 2012
dbSNP: rs1146586
rs1146586
1 1 75762289 intron variant C/A,T snp 3.3E-02 0.700 1 2012 2012
dbSNP: rs11574121
rs11574121
VDR
1 12 47844145 3 prime UTR variant G/A snp 1.6E-03 0.700 1 2012 2012
dbSNP: rs11621792
rs11621792
1 14 24402720 intron variant C/T snp 0.32 0.700 1 2015 2015
dbSNP: rs11638450
rs11638450
1 15 80898191 intron variant C/T snp 0.34 0.700 1 2014 2014
dbSNP: rs1169314
rs1169314
1 12 121005313 intron variant A/C,G snp 0.27 0.700 1 2015 2015
dbSNP: rs117492019
rs117492019
1 19 58170494 intergenic variant G/T snp 0.14 0.700 1 2015 2015
dbSNP: rs11784833
rs11784833
1 8 143989244 intron variant T/C snp 0.28 0.700 1 2015 2015
dbSNP: rs11800231
rs11800231
1 1 55052267 non coding transcript exon variant G/A,T snp 5.2E-02; 4.0E-06 7.7E-02; 3.2E-05 0.700 1 2013 2013