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: rs9268402
rs9268402
5 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.700 1.000 2 2008 2012
dbSNP: rs1265757
rs1265757
1 1.000 0.040 6 32334605 intron variant C/T snv 6.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs2281276
rs2281276
1 1.000 0.040 6 32372329 intron variant A/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs28361060
rs28361060
1 1.000 0.040 6 32336071 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs28366178
rs28366178
1 1.000 0.040 6 32308498 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs6910071
rs6910071
7 0.790 0.320 6 32315077 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs6913309
rs6913309
1 1.000 0.040 6 32372063 intron variant T/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs9268145
rs9268145
2 0.925 0.160 6 32289507 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9268362
rs9268362
2 0.925 0.160 6 32365564 intron variant A/G snv 0.16 0.15 0.700 1.000 1 2012 2012
dbSNP: rs9268400
rs9268400
1 1.000 0.040 6 32372877 intron variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs9268401
rs9268401
1 1.000 0.040 6 32373541 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs9268403
rs9268403
6 0.807 0.240 6 32373696 intron variant T/C snv 0.24 0.700 1.000 1 2012 2012