Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2758605 1 156230654 intron variant G/C snv 0.37 1
rs2758607 1 156232968 intron variant G/A;T snv 1
rs2758608 1 156233069 intron variant A/G;T snv 1
rs2758609 1 156233077 intron variant G/A snv 0.34 1
rs2758615 1 156188576 downstream gene variant T/C snv 0.43 1
rs2758616 1 156190567 upstream gene variant T/C snv 0.42 1
rs2758618 1 156191101 upstream gene variant T/C;G snv 1
rs2758619 1 156192768 upstream gene variant A/G snv 0.42 1
rs2842857 1 156198945 non coding transcript exon variant T/C snv 0.43 1
rs2842864 1 156189426 upstream gene variant G/A;C snv 1
rs2842865 1 156189741 upstream gene variant G/A snv 0.42 1
rs2842869 1 156190905 upstream gene variant A/G snv 0.42 1
rs2842873 1 156234862 intron variant C/G;T snv 1
rs2842882 1 156195551 intron variant T/A;G snv 1
rs2853643 1 156215040 intron variant G/A snv 0.30 1
rs2853646 1 156219835 intron variant C/T snv 0.30 1
rs2984613 1 156227589 intron variant C/T snv 0.32 1
rs2984615 1 156195526 intron variant G/C snv 0.42 1
rs3001789 1 156227823 intron variant T/G snv 0.37 1
rs3001790 1 156195499 intron variant T/G snv 0.42 1
rs6427304 1 156186998 intergenic variant A/G snv 0.43 1
rs6427307 1 156220292 intron variant A/G;T snv 1
rs7534434 1 156216824 intron variant A/G;T snv 1
rs887953 1 156221358 intron variant T/C snv 0.36 1
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97