Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 20 | |
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 15 | ||
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 11 | ||
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 10 | ||
rs12153855 | 0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 | 10 | ||
rs405509 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 8 | ||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 8 | ||
rs2269426 | 0.807 | 0.280 | 6 | 32108722 | intron variant | G/A | snv | 0.35 | 8 | ||
rs12678919 | 0.882 | 0.080 | 8 | 19986711 | intergenic variant | A/G | snv | 1.0E-01 | 7 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 5 | |
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 5 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 5 | ||
rs2043085 | 0.827 | 0.080 | 15 | 58388755 | intron variant | T/C | snv | 0.54 | 4 | ||
rs9391734 | 0.882 | 0.160 | 6 | 32130206 | 5 prime UTR variant | G/A | snv | 0.11 | 4 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 4 | ||
rs708272 | 0.708 | 0.440 | 16 | 56962376 | intron variant | G/A | snv | 0.42 | 0.38 | 4 | |
rs6795735 | 0.882 | 0.120 | 3 | 64719689 | intron variant | C/A;G;T | snv | 3 | |||
rs2303790 | 0.724 | 0.280 | 16 | 56983380 | missense variant | A/G | snv | 2.6E-03 | 6.5E-04 | 3 | |
rs5882 | 0.649 | 0.400 | 16 | 56982180 | missense variant | G/A;C | snv | 0.62 | 3 | ||
rs6680396 | 1.000 | 0.040 | 1 | 196663340 | intron variant | A/G | snv | 0.22 | 3 | ||
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 3 | |
rs406936 | 0.882 | 0.240 | 6 | 31965384 | intron variant | G/A | snv | 0.19 | 3 |