Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 13 | ||
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 10 | ||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 7 | ||
rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 7 | ||
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 6 | ||
rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
rs1142 | 0.851 | 0.040 | 7 | 105115879 | intron variant | C/T | snv | 0.31 | 6 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 6 | ||
rs2043085 | 0.827 | 0.080 | 15 | 58388755 | intron variant | T/C | snv | 0.54 | 6 | ||
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 6 | |||
rs10033900 | 0.807 | 0.040 | 4 | 109737911 | intron variant | T/C | snv | 0.54 | 5 | ||
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs11755724 | 0.807 | 0.320 | 6 | 7118757 | intron variant | A/G;T | snv | 5 | |||
rs1410996 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 5 | ||
rs570618 | 0.827 | 0.040 | 1 | 196687934 | intron variant | T/G | snv | 0.69 | 5 | ||
rs62358361 | 0.851 | 0.040 | 5 | 39327786 | intron variant | G/C;T | snv | 5 | |||
rs72802342 | 0.851 | 0.040 | 16 | 75200974 | downstream gene variant | C/A | snv | 6.2E-02 | 5 | ||
rs73036519 | 0.851 | 0.040 | 19 | 45245104 | intron variant | G/A;C | snv | 5 | |||
rs10781182 | 0.851 | 0.040 | 9 | 74002804 | intergenic variant | T/G | snv | 0.54 | 4 | ||
rs114092250 | 0.851 | 0.040 | 5 | 35494346 | intergenic variant | G/A;T | snv | 4 | |||
rs114254831 | 0.827 | 0.040 | 6 | 32187804 | intron variant | A/G | snv | 4 | |||
rs116503776 | 0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv | 4 | |||
rs11884770 | 0.851 | 0.040 | 2 | 227222204 | intron variant | T/A;C | snv | 4 |