Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3025021 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs833068 0.851 0.120 6 43774790 non coding transcript exon variant G/A snv 0.36 4
rs3024997 0.882 0.120 6 43777370 non coding transcript exon variant G/A snv 0.31 3
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs3025020 0.882 0.240 6 43781373 non coding transcript exon variant C/T snv 0.24 3
rs735286 6 43776884 non coding transcript exon variant C/T snv 0.23 1
rs3025000 1.000 0.120 6 43778432 non coding transcript exon variant C/T snv 0.29 0.23 1
rs3025033 0.807 0.360 6 43783338 non coding transcript exon variant A/G snv 0.18 6
rs3025040 0.882 0.120 6 43785314 3 prime UTR variant C/T snv 0.15 3
rs3025035 0.851 0.240 6 43783622 non coding transcript exon variant C/T snv 0.14 4
rs3025030 0.882 0.200 6 43782850 non coding transcript exon variant G/C snv 0.13 3
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3025053 0.925 0.120 6 43785588 3 prime UTR variant G/A snv 8.6E-02 2
rs3024994 0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs777846438 0.925 0.240 6 43780801 splice region variant C/T snv 4.4E-05 6.3E-05 2
rs140461341 6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs376388064 6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1
rs554561071 6 43777513 missense variant A/G snv 1.2E-05 3.5E-05 1
rs1212415280 6 43771130 missense variant G/T snv 2.1E-05 2