Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7741604 | 0.925 | 0.120 | 6 | 20731293 | intron variant | A/C;T | snv | 2 | |||
rs16859788 | 1.000 | 0.040 | 4 | 46969992 | intron variant | A/C;T | snv | 1 | |||
rs971257 | 1.000 | 0.040 | 2 | 167782126 | intergenic variant | A/C;T | snv | 0.53 | 1 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs80338945 | 0.695 | 0.440 | 13 | 20189313 | missense variant | A/G | snv | 6.4E-04 | 6.4E-04 | 32 | |
rs148881970 | 0.724 | 0.360 | 17 | 42543840 | missense variant | A/G | snv | 5.4E-05 | 1.3E-04 | 22 | |
rs1060499733 | 0.851 | 0.120 | 3 | 47846757 | missense variant | A/G | snv | 11 | |||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 9 | ||
rs736707 | 0.851 | 0.040 | 7 | 103489956 | intron variant | A/G | snv | 0.30 | 6 | ||
rs12456492 | 0.882 | 0.080 | 18 | 43093415 | intron variant | A/G | snv | 0.33 | 3 | ||
rs155806 | 1.000 | 0.040 | 5 | 140970255 | intron variant | A/G | snv | 8.9E-02 | 2 | ||
rs753426385 | 0.925 | 0.120 | Y | 14840846 | missense variant | A/G | snv | 2 | |||
rs879254129 | 0.925 | 0.040 | 12 | 13562977 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs9635542 | 1.000 | 0.040 | 16 | 4951379 | intron variant | A/G | snv | 0.11 | 2 | ||
rs10500171 | 1.000 | 0.040 | 7 | 147183313 | intron variant | A/G | snv | 0.52 | 1 | ||
rs1057518999 | 1.000 | 0.040 | 3 | 70977826 | splice donor variant | A/G | snv | 1 | |||
rs10732392 | 1.000 | 0.040 | 9 | 126633758 | intron variant | A/G | snv | 0.84 | 1 | ||
rs11102807 | 1.000 | 0.040 | 1 | 114518963 | intergenic variant | A/G | snv | 0.44 | 1 | ||
rs12336217 | 1.000 | 0.040 | 9 | 126637591 | intron variant | A/G | snv | 0.17 | 1 | ||
rs12518194 | 1.000 | 0.040 | 5 | 25951452 | intergenic variant | A/G | snv | 0.27 | 1 | ||
rs1408744 | 1.000 | 0.040 | 6 | 23789887 | intergenic variant | A/G | snv | 0.63 | 1 | ||
rs1426217 | 1.000 | 0.040 | 15 | 26575978 | intron variant | A/G | snv | 0.46 | 1 |