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 | ||
rs2306235 | 0.827 | 0.040 | 1 | 150150942 | missense variant | C/G;T | snv | 1.1E-02; 1.6E-05 | 4.4E-03 | 6 | |
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 | |
rs13058338 | 1.000 | 0.040 | 22 | 37236730 | intron variant | T/A;G | snv | 4 | |||
rs1553265736 | 0.925 | 0.040 | 1 | 156136080 | missense variant | G/C | snv | 4 | |||
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 | ||
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 | |||
rs200536955 | 0.925 | 0.040 | 19 | 35756980 | missense variant | G/A;T | snv | 7.0E-04 | 3 | ||
rs3829365 | 0.925 | 0.040 | 13 | 37598759 | 5 prime UTR variant | G/A;C | snv | 4.0E-06; 0.11 | 3 | ||
rs6026584 | 0.925 | 0.040 | 20 | 58894018 | intron variant | T/C | snv | 0.70 | 3 | ||
rs749303395 | 0.882 | 0.040 | 1 | 114680329 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 3 | ||
rs794728602 | 1.000 | 0.040 | 1 | 156115168 | missense variant | G/A | snv | 3 | |||
rs958546 | 0.882 | 0.040 | 13 | 46259582 | intron variant | G/C | snv | 0.29 | 3 | ||
rs10932374 | 0.925 | 0.040 | 2 | 211379678 | 3 prime UTR variant | G/A | snv | 0.23 | 2 | ||
rs13003941 | 0.925 | 0.040 | 2 | 211378978 | 3 prime UTR variant | G/C;T | snv | 0.26 | 2 |