Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9987289 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs12286037 1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs711752 1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs9939224 1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs11820589 1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 4
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 4
rs481843 1.000 0.040 11 116655150 non coding transcript exon variant C/T snv 8.8E-02 4
rs6494005 1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4
rs12686004 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 3
rs16940212 1.000 0.040 15 58401821 intron variant G/A;T snv 3
rs17863787 0.925 0.040 2 233702448 intron variant T/G snv 0.30 3
rs263
LPL
1.000 0.040 8 19955301 intron variant C/T snv 0.23 3
rs271
LPL
1.000 0.040 8 19956191 intron variant G/A;T snv 3
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 3
rs486394 1.000 0.040 11 116655605 intron variant A/C;T snv 3
rs7013777 1.000 0.040 8 20020845 intergenic variant T/C;G snv 3
rs7461115 1.000 0.040 8 20014029 intergenic variant C/A;G snv 0.37 3
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 3
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 2