Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 27 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 18 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 12 | ||
rs5015480 | 0.851 | 0.120 | 10 | 92705802 | downstream gene variant | C/T | snv | 0.42 | 9 | ||
rs12243326 | 0.925 | 0.160 | 10 | 113029056 | intron variant | T/C | snv | 0.27 | 5 | ||
rs7936247 | 1.000 | 0.040 | 11 | 92956866 | intergenic variant | G/T | snv | 0.37 | 5 | ||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 4 | ||||
rs7102710 | 11 | 14244067 | intron variant | T/C | snv | 0.10 | 3 | ||||
rs17271340 | 15 | 62055686 | intron variant | C/T | snv | 0.33 | 2 | ||||
rs2042608 | 15 | 61940181 | intron variant | C/A | snv | 0.48 | 2 | ||||
rs4746822 | 10 | 69223185 | non coding transcript exon variant | C/T | snv | 0.59 | 2 | ||||
rs927332 | 6 | 6331640 | intergenic variant | T/C | snv | 0.48 | 2 | ||||
rs13421358 | 2 | 43020088 | regulatory region variant | C/T | snv | 0.40 | 1 | ||||
rs17271305 | 15 | 62040781 | intron variant | A/G;T | snv | 1 | |||||
rs7330796 | 13 | 75324027 | intron variant | T/C | snv | 0.76 | 1 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs17681684 | 17 | 9889451 | missense variant | G/A;C | snv | 0.22; 4.0E-06 | 1 | ||||
rs150112597 | 2 | 176189453 | missense variant | G/C;T | snv | 2.4E-03; 4.1E-06 | 1 | ||||
rs3741151 | 11 | 73309801 | missense variant | G/A;C;T | snv | 8.1E-06; 8.0E-02 | 1 | ||||
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 37 | ||
rs201111080 | 1 | 176670971 | missense variant | G/T | snv | 1.9E-04 | 1.8E-04 | 1 | |||
rs78714016 | 17 | 7078084 | missense variant | G/A;T | snv | 4.0E-03 | 1 | ||||
rs17683011 | 1.000 | 0.120 | 22 | 32049959 | missense variant | A/G | snv | 4.8E-02 | 4.5E-02 | 3 |