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: rs1006725
rs1006725
2 10 112970444 intron variant A/G snv 4.2E-03 0.700 1.000 1 2012 2012
dbSNP: rs10087178
rs10087178
2 8 10111284 intron variant T/C snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10212320
rs10212320
2 3 30632373 non coding transcript exon variant C/T snv 7.2E-03 0.700 1.000 1 2012 2012
dbSNP: rs10306121
rs10306121
2 9 122372369 intron variant A/T snv 6.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs10433493
rs10433493
2 3 190647811 intron variant G/C snv 1.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs10495399
rs10495399
2 1 237648783 intron variant T/G snv 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs11075663
rs11075663
2 16 67935887 intron variant T/G snv 3.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs11192141
rs11192141
2 10 82005843 intron variant G/A snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs1144302
rs1144302
F3
2 1 94534558 intron variant C/T snv 4.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs1146586
rs1146586
2 1 75762289 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11574121
rs11574121
VDR
2 12 47844145 3 prime UTR variant G/A snv 1.5E-03 0.700 1.000 1 2012 2012
dbSNP: rs11800231
rs11800231
2 1 55052267 non coding transcript exon variant G/A;T snv 5.2E-02; 4.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs11809491
rs11809491
2 1 65954975 intron variant G/T snv 2.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs11813704
rs11813704
2 10 107102114 intron variant G/T snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs11854545
rs11854545
2 15 88825873 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11908397
rs11908397
2 20 31822508 intron variant G/A snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs1329980
rs1329980
2 1 91789389 intron variant T/C snv 1.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1365771
rs1365771
2 15 58568503 intron variant T/A snv 0.96 0.700 1.000 1 2012 2012
dbSNP: rs1407717
rs1407717
2 1 116370991 upstream gene variant T/C snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs1571980
rs1571980
2 1 237664204 intron variant T/C snv 1.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs16856594
rs16856594
2 2 169197702 intron variant G/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs16860953
rs16860953
2 1 162364127 5 prime UTR variant G/A snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs16884688
rs16884688
2 6 21220145 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs16891227
rs16891227
2 8 42328508 intron variant C/T snv 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs16902608
rs16902608
2 5 87275476 intron variant A/G snv 8.5E-03 0.700 1.000 1 2012 2012