Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1387153 | 0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv | 10 | |||
rs1483121 | 1.000 | 0.080 | 11 | 48311808 | downstream gene variant | G/A | snv | 9.7E-02 | 4 | ||
rs10747083 | 12 | 132465032 | downstream gene variant | G/A;T | snv | 2 | |||||
rs35859536 | 8 | 117179236 | downstream gene variant | C/T | snv | 0.25 | 2 | ||||
rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 4 | ||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 5 | ||
rs2292910 | 1.000 | 0.080 | 11 | 45882062 | 3 prime UTR variant | A/C | snv | 0.66 | 3 | ||
rs3778321 | 6 | 7250037 | 3 prime UTR variant | G/A | snv | 0.11 | 2 | ||||
rs174550 | 0.925 | 0.160 | 11 | 61804006 | 5 prime UTR variant | T/C | snv | 0.28 | 13 | ||
rs11603334 | 1.000 | 0.080 | 11 | 72721940 | 5 prime UTR variant | G/A | snv | 0.12 | 5 | ||
rs1552224 | 1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 | 4 | ||
rs2280231 | 11 | 47578886 | 5 prime UTR variant | C/T | snv | 0.24 | 0.20 | 2 | |||
rs11715915 | 3 | 49417897 | synonymous variant | C/A;T | snv | 0.28 | 2 | ||||
rs174537 | 0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 | 23 | ||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 7 | ||
rs17762454 | 0.925 | 0.120 | 6 | 7212967 | non coding transcript exon variant | C/T | snv | 0.25 | 4 | ||
rs16980051 | 19 | 45842628 | non coding transcript exon variant | T/A;C | snv | 0.47 | 2 | ||||
rs753993 | 11 | 47328418 | non coding transcript exon variant | C/A | snv | 0.33 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs2657879 | 1.000 | 0.080 | 12 | 56471554 | missense variant | A/G | snv | 0.17 | 0.15 | 9 | |
rs17265513 | 0.925 | 0.160 | 20 | 41203988 | missense variant | T/C | snv | 0.14 | 0.14 | 6 | |
rs1124649 | 2 | 27037601 | missense variant | G/A | snv | 0.32 | 0.35 | 2 | |||
rs12440695 | 15 | 62142957 | regulatory region variant | T/C | snv | 0.32 | 3 | ||||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 |