Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1276184054 0.851 0.080 7 55201305 missense variant G/A snv 4.0E-06 4
rs776375114 0.851 0.080 7 55202577 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs1389500636 0.827 0.080 7 55156796 missense variant G/A snv 6
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs2072454 0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs1057519911 0.776 0.160 22 21772875 missense variant C/T snv 10
rs3136038 0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36 13
rs3813867 0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs2233678 0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs745564626 0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs755174338 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 15
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32