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: rs10160659
rs10160659
1 1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs17044542
rs17044542
1 1.000 0.080 3 6299812 intron variant A/C snv 5.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs2647046
rs2647046
3 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 0.700 1.000 1 2009 2009
dbSNP: rs2839750
rs2839750
1 1.000 0.080 2 52901952 intron variant A/C snv 3.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs2858884
rs2858884
2 0.925 0.200 6 32732306 upstream gene variant A/C snv 0.23 0.800 1.000 1 2010 2010
dbSNP: rs7175718
rs7175718
3 0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs7187262
rs7187262
1 1.000 0.080 16 69460376 intron variant A/C snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs7579759
rs7579759
1 1.000 0.080 2 28470781 intron variant A/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs9270986
rs9270986
3 0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 0.700 1.000 1 2009 2009
dbSNP: rs9373298
rs9373298
1 1.000 0.080 6 141198693 regulatory region variant A/C snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs10226621
rs10226621
1 1.000 0.080 7 4068008 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs17138435
rs17138435
3 0.882 0.120 11 79481943 TF binding site variant A/C;G snv 1.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs686881
rs686881
1 1.000 0.080 18 54287164 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs7105164
rs7105164
1 1.000 0.080 11 12132546 intron variant A/C;G snv 5.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs6023560
rs6023560
3 0.882 0.120 20 54743554 intergenic variant A/C;G;T snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs10775354
rs10775354
1 1.000 0.080 16 6757689 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs539703
rs539703
4 0.882 0.200 6 32320685 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9267954
rs9267954
3 0.882 0.200 6 32245275 regulatory region variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10091183
rs10091183
1 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs1009449
rs1009449
1 1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 0.700 1.000 1 2009 2009
dbSNP: rs10956273
rs10956273
1 1.000 0.080 8 125953914 non coding transcript exon variant A/G snv 6.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs11574049
rs11574049
VDR
1 1.000 0.080 12 47878732 intron variant A/G snv 1.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11697253
rs11697253
1 1.000 0.080 20 25014378 intron variant A/G snv 9.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs1201324
rs1201324
1 1.000 0.080 13 89601725 intron variant A/G snv 0.98 0.700 1.000 1 2009 2009
dbSNP: rs12695894
rs12695894
3 0.882 0.120 3 148724853 intron variant A/G snv 2.7E-02 0.700 1.000 1 2009 2009