Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12210050 | 0.807 | 0.040 | 6 | 475489 | non coding transcript exon variant | C/T | snv | 0.11 | 8 | ||
rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 7 | ||
rs1024708183 | 0.925 | 0.040 | 19 | 7909761 | missense variant | A/G | snv | 4 | |||
rs10754833 | 0.851 | 0.040 | 1 | 236021631 | intron variant | T/A;C | snv | 4 | |||
rs1057519805 | 1.000 | 0.040 | 15 | 66436839 | missense variant | T/C | snv | 3 | |||
rs1110400 | 1.000 | 0.040 | 16 | 89919722 | missense variant | T/C | snv | 5.6E-03 | 6.6E-03 | 3 | |
rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
rs397507482 | 0.882 | 0.040 | 7 | 140753386 | missense variant | A/C | snv | 3 | |||
rs700635 | 0.925 | 0.040 | 2 | 201288502 | 3 prime UTR variant | C/A | snv | 0.72 | 3 | ||
rs749496294 | 0.925 | 0.040 | 20 | 3562435 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 3 | |
rs766310650 | 1.000 | 0.040 | 6 | 36677906 | 5 prime UTR variant | T/C | snv | 6.2E-05 | 2.1E-05 | 3 | |
rs1057519702 | 1.000 | 0.040 | 4 | 54726020 | missense variant | T/C | snv | 2 | |||
rs1057519708 | 1.000 | 0.040 | 4 | 54728096 | missense variant | T/A;G | snv | 2 | |||
rs1057519730 | 1.000 | 0.040 | 15 | 66436786 | missense variant | T/A;G | snv | 2 | |||
rs1057519731 | 0.925 | 0.040 | 15 | 66436816 | missense variant | G/C | snv | 2 | |||
rs1057519804 | 1.000 | 0.040 | 14 | 104776711 | missense variant | G/T | snv | 2 | |||
rs1057519808 | 1.000 | 0.040 | 19 | 4117543 | missense variant | T/G | snv | 2 | |||
rs1057519837 | 1.000 | 0.040 | 3 | 41224631 | missense variant | C/G;T | snv | 2 | |||
rs1057519856 | 0.925 | 0.040 | 15 | 66436815 | missense variant | T/A | snv | 2 | |||
rs1057520031 | 1.000 | 0.040 | 4 | 54727440 | missense variant | A/C;G | snv | 2 | |||
rs11547464 | 1.000 | 0.040 | 16 | 89919683 | missense variant | G/A | snv | 5.3E-03 | 4.7E-03 | 2 | |
rs1204552 | 1.000 | 0.040 | 20 | 36050981 | non coding transcript exon variant | T/A;C;G | snv | 2 | |||
rs121909233 | 1.000 | 0.040 | 10 | 87864524 | missense variant | G/A | snv | 2 | |||
rs121913323 | 1.000 | 0.040 | 19 | 1220416 | stop gained | C/T | snv | 2 | |||
rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 2 |