Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 | ||
rs57045855 | 0.882 | 0.040 | 1 | 156134464 | missense variant | A/G;T | snv | 6 | |||
rs737337 | 0.925 | 0.040 | 19 | 11236817 | synonymous variant | T/C | snv | 0.15 | 0.20 | 6 | |
rs12564445 | 0.851 | 0.040 | 1 | 201376359 | intron variant | G/A | snv | 0.27 | 5 | ||
rs535039125 | 0.851 | 0.040 | 19 | 41004380 | missense variant | C/T | snv | 1.1E-04 | 1.3E-04 | 5 | |
rs1739843 | 0.882 | 0.040 | 1 | 16016759 | intron variant | T/C | snv | 0.62 | 4 | ||
rs198358 | 0.925 | 0.040 | 1 | 11844019 | 3 prime UTR variant | T/C | snv | 0.32 | 4 | ||
rs61661343 | 0.851 | 0.040 | 1 | 156130687 | missense variant | T/C | snv | 4 | |||
rs9351814 | 0.882 | 0.040 | 6 | 71484004 | intergenic variant | A/C | snv | 0.35 | 4 | ||
rs1028728 | 0.925 | 0.040 | 13 | 37599679 | upstream gene variant | A/T | snv | 0.20 | 3 | ||
rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 | ||
rs11006544 | 1.000 | 0.040 | 10 | 59510886 | intergenic variant | T/C | snv | 7.3E-03 | 3 | ||
rs11110004 | 1.000 | 0.040 | 12 | 99694540 | intron variant | T/C | snv | 5.1E-03 | 3 | ||
rs112434206 | 1.000 | 0.040 | 5 | 33083283 | intron variant | A/C;G | snv | 7.6E-03 | 3 | ||
rs113235453 | 1.000 | 0.040 | 14 | 31849939 | intron variant | A/G | snv | 3.5E-02 | 3 | ||
rs114821210 | 1.000 | 0.040 | 5 | 166089843 | intergenic variant | C/A | snv | 6.0E-03 | 3 | ||
rs12362161 | 1.000 | 0.040 | 11 | 98834502 | intergenic variant | C/A;G | snv | 3 | |||
rs1249958 | 0.925 | 0.040 | 12 | 54582053 | missense variant | C/T | snv | 2.7E-02 | 3 | ||
rs1258130495 | 0.882 | 0.040 | 4 | 147485727 | missense variant | G/A | snv | 3 | |||
rs1303946678 | 0.925 | 0.040 | 22 | 42126851 | missense variant | C/G | snv | 3 | |||
rs139130723 | 1.000 | 0.040 | 6 | 14411553 | intergenic variant | A/G | snv | 4.4E-03 | 3 | ||
rs142803096 | 1.000 | 0.040 | 6 | 14420151 | intergenic variant | G/C | snv | 4.4E-03 | 3 | ||
rs144303414 | 1.000 | 0.040 | 18 | 48509413 | intergenic variant | A/C | snv | 1.5E-02 | 3 | ||
rs148133894 | 1.000 | 0.040 | 16 | 24584678 | intergenic variant | T/C | snv | 2.4E-03 | 3 | ||
rs149322277 | 1.000 | 0.040 | 16 | 87925065 | intron variant | C/T | snv | 5.6E-03 | 3 |