Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 11 | |
rs1837253 | 0.790 | 0.240 | 5 | 111066174 | upstream gene variant | T/C | snv | 0.72 | 8 | ||
rs34290285 | 0.851 | 0.120 | 2 | 241759225 | intron variant | G/A | snv | 0.27 | 8 | ||
rs17622378 | 0.790 | 0.200 | 5 | 132442760 | intron variant | A/G | snv | 0.28 | 8 | ||
rs7302200 | 0.851 | 0.200 | 12 | 56055651 | regulatory region variant | G/A | snv | 0.23 | 6 | ||
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 6 | ||
rs56062135 | 0.790 | 0.200 | 15 | 67163292 | intron variant | C/T | snv | 0.18 | 6 | ||
rs72743461 | 0.827 | 0.160 | 15 | 67149412 | intron variant | C/A;T | snv | 6 | |||
rs117710327 | 0.882 | 0.080 | 19 | 33235672 | TF binding site variant | C/A | snv | 5.0E-02 | 5 | ||
rs7936312 | 0.882 | 0.080 | 11 | 76582682 | intergenic variant | G/T | snv | 0.44 | 5 | ||
rs2428494 | 0.827 | 0.160 | 6 | 31354420 | intron variant | T/A;C | snv | 5 | |||
rs705699 | 0.882 | 0.160 | 12 | 55991020 | non coding transcript exon variant | G/A | snv | 0.40 | 5 | ||
rs10414065 | 0.882 | 0.080 | 19 | 33230549 | upstream gene variant | C/T | snv | 5.5E-02 | 4 | ||
rs10667251 | 0.925 | 0.080 | 17 | 49388381 | intron variant | -/TCT | delins | 0.47 | 4 | ||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 4 | ||
rs62322662 | 0.925 | 0.080 | 4 | 122438414 | intergenic variant | A/G | snv | 5.1E-02 | 4 | ||
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 4 | ||
rs12470864 | 0.925 | 0.080 | 2 | 102309902 | upstream gene variant | G/A | snv | 0.30 | 4 | ||
rs72823641 | 0.882 | 0.080 | 2 | 102319699 | intron variant | T/A;C | snv | 4 | |||
rs12722502 | 0.882 | 0.080 | 10 | 6051176 | intron variant | C/T | snv | 7.8E-03 | 4 | ||
rs3122929 | 0.882 | 0.080 | 12 | 57115319 | intron variant | C/T | snv | 0.33 | 4 | ||
rs1775554 | 0.882 | 0.080 | 10 | 9012377 | intergenic variant | A/C | snv | 0.35 | 3 | ||
rs4739738 | 0.882 | 0.120 | 8 | 80379410 | intron variant | G/A | snv | 0.60 | 3 | ||
rs992969 | 0.882 | 0.080 | 9 | 6209697 | intergenic variant | A/G;T | snv | 3 | |||
rs35441874 | 0.882 | 0.120 | 16 | 11119164 | intron variant | T/A | snv | 0.19 | 3 |