Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs79105258 12 111280427 intron variant C/A;T snv 23
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs13108218 4 3442204 intron variant A/G;T snv 7
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs77924615 1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs7832708 8 10332530 intron variant C/T snv 0.49 4
rs10254101 7 151718450 intron variant C/T snv 0.23 3
rs2290263 7 25847658 intergenic variant G/A snv 0.77 3
rs11636251 15 75946679 intron variant C/T snv 0.42 2
rs72683923 14 50269229 synonymous variant T/C snv 1.0E-02 9.9E-03 2