Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs563558831 0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs2812378 0.790 0.200 9 34710263 intron variant G/A;C snv 8
rs582757 0.776 0.320 6 137876687 intron variant C/T snv 0.70 8
rs6651252 0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs71624119 0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 7
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs2451258 0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs74956615 0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 6