Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs1980493 0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs3134942 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs660895 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6