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: rs682938
rs682938
1 1.000 0.040 15 48572170 intron variant A/G snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs714290
rs714290
1 1.000 0.040 15 48459132 intron variant C/G snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs7184016
rs7184016
1 1.000 0.040 15 48518302 intron variant G/T snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs8026752
rs8026752
1 1.000 0.040 15 48531573 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs8034591
rs8034591
1 1.000 0.040 15 48432571 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs8034829
rs8034829
1 1.000 0.040 15 48513830 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs8041668
rs8041668
1 1.000 0.040 15 48543158 intron variant T/C snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs920184
rs920184
1 1.000 0.040 15 48600742 intron variant C/T snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs9806163
rs9806163
1 1.000 0.040 15 48511642 intron variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs9806323
rs9806323
1 1.000 0.040 15 48473818 intron variant T/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs595244
rs595244
3 0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 0.700 1.000 1 2016 2016