Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35324266 1.000 0.040 6 32625467 upstream gene variant C/T snv 0.16 1
rs62209647 1.000 0.040 20 33917852 upstream gene variant G/C snv 4.4E-02 1
rs6791479 1.000 0.040 3 189487243 intergenic variant T/A snv 0.48 1
rs7097008 1.000 0.040 10 67849782 non coding transcript exon variant C/A snv 0.60 1
rs9557210 1.000 0.040 13 99395250 intergenic variant G/A snv 0.16 1
rs9651495 1.000 0.040 10 89172624 regulatory region variant G/A snv 0.13 1
rs774121564 1.000 0.040 2 275197 missense variant C/G snv 4.1E-06 1
rs117984432 1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02 1
rs1460816 1.000 0.040 13 32354271 intron variant G/A snv 0.54 1
rs116150891 1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03 1
rs115169993 1.000 0.040 1 162772032 missense variant G/A snv 7.8E-04 2.9E-03 1
rs8063761 1.000 0.040 16 89961218 intron variant A/T snv 0.33 1
rs9383064 1.000 0.040 6 15535090 intron variant G/C snv 0.24 1
rs121913230 1.000 0.040 7 55181437 missense variant G/A snv 1
rs121913431 1.000 0.040 7 55181438 missense variant G/A snv 1
rs779759678 1.000 0.040 3 36993556 missense variant C/G snv 4.0E-06 3.5E-05 1
rs2233914 1.000 0.040 9 113221260 5 prime UTR variant G/A snv 0.16 0.13 1
rs6743068 1.000 0.040 2 201289197 intron variant A/G snv 0.72 1
rs62246017 1.000 0.040 3 71433933 intron variant G/A;C snv 1
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs10818524
GSN
1.000 0.040 9 121267901 intron variant T/C snv 0.37 1
rs45549733 1.000 0.040 11 67586503 missense variant C/G;T snv 7.6E-05 1
rs4455710 1.000 0.040 6 32641081 intron variant C/T snv 0.22 1
rs879576 1.000 0.040 22 17108356 missense variant G/A;C snv 0.11 1
rs454421 1.000 0.040 19 45341392 intron variant C/G;T snv 0.44 1