Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2232365 | 0.716 | 0.480 | X | 49259429 | intron variant | T/C | snv | 16 | |||
rs3117582 | 0.716 | 0.440 | 6 | 31652743 | intron variant | T/G | snv | 7.1E-02 | 14 | ||
rs1800012 | 0.763 | 0.320 | 17 | 50200388 | intron variant | C/A | snv | 0.14 | 13 | ||
rs1143633 | 0.752 | 0.280 | 2 | 112832890 | intron variant | C/G;T | snv | 11 | |||
rs2082940 | 0.763 | 0.480 | 3 | 186856375 | 3 prime UTR variant | T/A;C | snv | 10 | |||
rs1194611372 | 0.763 | 0.320 | 1 | 152032679 | missense variant | A/C | snv | 9 | |||
rs121913474 | 0.790 | 0.200 | 10 | 121515260 | missense variant | A/G | snv | 9 | |||
rs1456315 | 0.790 | 0.200 | 8 | 127091692 | non coding transcript exon variant | T/A;C | snv | 9 | |||
rs12149832 | 0.851 | 0.120 | 16 | 53808996 | intron variant | G/A | snv | 0.31 | 8 | ||
rs16901946 | 0.827 | 0.160 | 8 | 127088680 | non coding transcript exon variant | A/G | snv | 1.7E-02 | 8 | ||
rs5030772 | 0.790 | 0.320 | 1 | 172664210 | intron variant | A/G | snv | 9.9E-02 | 7 | ||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 7 | ||
rs650108 | 0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 | 6 | ||
rs8044769 | 0.851 | 0.200 | 16 | 53805223 | intron variant | T/A;C;G | snv | 6 | |||
rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
rs121918505 | 0.851 | 0.080 | 10 | 121520119 | missense variant | A/G | snv | 5 | |||
rs12885713 | 0.827 | 0.200 | 14 | 90397013 | intron variant | C/A;G;T | snv | 5 | |||
rs2929970 | 0.827 | 0.200 | 8 | 133228894 | 3 prime UTR variant | G/A | snv | 0.52 | 5 | ||
rs7135617 | 0.827 | 0.240 | 12 | 121631099 | intron variant | T/C;G | snv | 5 | |||
rs12982744 | 0.925 | 0.040 | 19 | 2177194 | intron variant | C/A;G;T | snv | 4 | |||
rs17039192 | 0.851 | 0.120 | 2 | 46297441 | 5 prime UTR variant | C/T | snv | 1.9E-02 | 4 | ||
rs2057768 | 0.925 | 0.120 | 16 | 27310774 | upstream gene variant | C/A;G;T | snv | 4 | |||
rs2820436 | 0.882 | 0.040 | 1 | 219467338 | intergenic variant | A/C;G | snv | 4 | |||
rs10492367 | 0.882 | 0.040 | 12 | 27862037 | regulatory region variant | G/T | snv | 0.12 | 3 | ||
rs10947262 | 0.925 | 0.040 | 6 | 32405535 | non coding transcript exon variant | C/T | snv | 0.12 | 3 |