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: rs12213249
rs12213249
1 6 10926709 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs2327323
rs2327323
1 6 10933580 intron variant C/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1359159
rs1359159
1 6 10934138 intron variant C/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1578068
rs1578068
1 6 10937871 intron variant T/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1225736
rs1225736
1 6 10939156 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs9393800
rs9393800
3 6 10951504 intron variant A/G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs1225741
rs1225741
1 6 10952010 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs9379969
rs9379969
1 6 10952403 intron variant T/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs1007323
rs1007323
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1225744
rs1225744
1 6 10954307 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs9393804
rs9393804
1 6 10955897 intron variant T/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs7759825
rs7759825
1 6 10956416 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs1225753
rs1225753
1 6 10956456 intron variant G/A snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs7773173
rs7773173
1 6 10956470 intron variant G/C snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs9368506
rs9368506
1 6 10958239 intron variant G/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs6918936
rs6918936
1 6 10959925 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs6920247
rs6920247
1 6 10959940 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4711146
rs4711146
1 6 10961172 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs9791208
rs9791208
1 6 10961416 intron variant T/C snv 0.24 0.19 0.700 1.000 1 2011 2011
dbSNP: rs2295600
rs2295600
1 6 10962017 intron variant A/G snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs7774711
rs7774711
1 6 10964788 intron variant A/G;T snv 0.700 1.000 1 2011 2011