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 | 1.000 | 0.040 | 9 | 121289122 | intron variant | A/G | snv | 0.70 | 1 | ||
rs10818524 | 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 |