Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830956 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 1
rs12545984 1.000 0.040 8 19989748 intergenic variant C/T snv 0.16 1
rs1441756 1.000 0.040 8 20010875 intergenic variant A/C;G;T snv 1
rs1522813 1.000 0.040 2 226080466 regulatory region variant G/A snv 0.29 1
rs180088 1.000 0.040 17 69951455 intergenic variant T/A;C snv 0.71 1
rs180344 1.000 0.040 11 116742468 regulatory region variant T/C snv 0.34 1
rs1837842 1.000 0.040 8 20010779 intergenic variant T/C snv 0.23 1
rs376021 1.000 0.040 1 161555218 intron variant T/C snv 1.5E-04 1
rs4244457 1.000 0.040 8 20041535 intergenic variant C/G;T snv 1
rs4442164 1.000 0.040 8 20034670 regulatory region variant A/G snv 0.28 1
rs4449813 1.000 0.040 8 20045809 intergenic variant G/A snv 0.34 1
rs6995374 1.000 0.040 8 10468602 intergenic variant C/G snv 0.22 1
rs916829 1.000 0.040 11 17418926 intron variant A/G;T snv 1
rs4766587 1.000 0.040 12 109247525 intron variant G/A snv 0.23 1
rs6606697 1.000 0.040 12 109173915 intron variant A/G snv 0.48 1
rs1324805 1.000 0.040 X 109719433 intron variant A/G snv 0.45 1
rs1133607 1.000 0.040 16 20483086 missense variant C/G;T snv 4.0E-06; 0.13 1
rs13010956 1.000 0.040 2 157556030 intron variant T/C snv 0.39 1
rs1259867035 1.000 0.040 3 186854387 stop gained C/T snv 4.0E-06 1
rs746639990 1.000 0.040 3 186854598 missense variant A/G snv 2.1E-04 7.0E-06 1
rs10920533 1.000 0.040 1 202956690 intron variant G/A snv 0.22 1
rs17055869 1.000 0.040 8 26740131 intergenic variant C/A;T snv 1
rs775276843
AGT
1.000 0.040 1 230710676 missense variant C/T snv 4.0E-06 1
rs11631342 1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 1
rs6511435 1.000 0.040 19 10103816 upstream gene variant T/A;C;G snv 1