Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1332099 | 0.724 | 0.240 | 10 | 99538694 | downstream gene variant | T/C;G | snv | 14 | |||
rs4869313 | 0.724 | 0.240 | 5 | 96888176 | intron variant | T/A;G | snv | 14 | |||
rs72928038 | 0.695 | 0.360 | 6 | 90267049 | intron variant | G/A | snv | 0.11 | 19 | ||
rs2066363 | 0.724 | 0.240 | 1 | 81771892 | intron variant | C/T | snv | 0.71 | 14 | ||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs72743477 | 0.724 | 0.240 | 15 | 67171953 | intron variant | A/G | snv | 0.17 | 14 | ||
rs2738774 | 0.724 | 0.240 | 20 | 63637985 | downstream gene variant | G/A;C | snv | 14 | |||
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs706778 | 0.695 | 0.320 | 10 | 6056986 | intron variant | C/T | snv | 0.46 | 15 | ||
rs7731626 | 0.716 | 0.240 | 5 | 56148856 | intron variant | G/A | snv | 0.30 | 15 | ||
rs1689510 | 0.724 | 0.240 | 12 | 56002984 | non coding transcript exon variant | G/C | snv | 0.25 | 16 | ||
rs117372389 | 0.724 | 0.240 | 16 | 50634166 | 3 prime UTR variant | G/T | snv | 1.1E-02 | 14 | ||
rs77150043 | 0.724 | 0.240 | 16 | 50270338 | intron variant | C/T | snv | 0.17 | 14 | ||
rs7672495 | 0.724 | 0.240 | 4 | 4990640 | regulatory region variant | T/C | snv | 0.21 | 14 | ||
rs36051895 | 0.716 | 0.240 | 9 | 4981866 | upstream gene variant | G/T | snv | 0.25 | 15 | ||
rs4625 | 0.716 | 0.280 | 3 | 49534707 | 3 prime UTR variant | A/G | snv | 0.30 | 17 | ||
rs602662 | 0.716 | 0.280 | 19 | 48703728 | missense variant | G/A | snv | 0.40 | 0.47 | 15 | |
rs7725052 | 0.716 | 0.240 | 5 | 40487168 | intron variant | C/T | snv | 0.52 | 15 | ||
rs17466626 | 0.724 | 0.240 | 12 | 40366829 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 14 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 15 | ||
rs2836882 | 0.724 | 0.240 | 21 | 39094644 | intergenic variant | G/A | snv | 0.23 | 15 | ||
rs7100025 | 0.724 | 0.240 | 10 | 37303610 | intron variant | G/A | snv | 0.68 | 14 | ||
rs114846446 | 0.724 | 0.240 | 2 | 2944140 | intron variant | G/A | snv | 9.5E-03 | 14 | ||
rs12928404 | 0.724 | 0.240 | 16 | 28835925 | splice region variant | T/C | snv | 0.44 | 0.45 | 15 |