Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2732875 | 0.790 | 0.080 | X | 9795858 | intron variant | C/G;T | snv | 9 | |||
rs5934683 | 0.790 | 0.080 | X | 9783434 | intron variant | T/C | snv | 0.50 | 9 | ||
rs764355898 | 1.000 | 0.080 | X | 105923145 | missense variant | A/C | snv | 7.9E-05 | 1.9E-05 | 1 | |
rs555607708 | 0.667 | 0.360 | 22 | 28695869 | frameshift variant | G/- | del | 2.0E-03 | 1.8E-03 | 33 | |
rs137853007 | 0.790 | 0.240 | 22 | 28725254 | missense variant | G/A;T | snv | 5.2E-05 | 9 | ||
rs5753618 | 0.790 | 0.080 | 22 | 31442532 | intron variant | C/T | snv | 0.20 | 9 | ||
rs11907546 | 0.708 | 0.280 | 20 | 34131991 | upstream gene variant | C/A;T | snv | 17 | |||
rs2300206 | 0.708 | 0.280 | 20 | 34002002 | intron variant | G/C;T | snv | 17 | |||
rs961253 | 0.732 | 0.240 | 20 | 6423634 | intergenic variant | C/A | snv | 0.34 | 15 | ||
rs4925386 | 0.776 | 0.080 | 20 | 62345988 | intron variant | T/C | snv | 0.56 | 14 | ||
rs6058093 | 0.776 | 0.080 | 20 | 34625392 | intron variant | A/C | snv | 0.55 | 12 | ||
rs2179593 | 0.790 | 0.080 | 20 | 44031646 | intron variant | C/A | snv | 0.71 | 11 | ||
rs2738783 | 0.763 | 0.160 | 20 | 63677259 | intron variant | T/G | snv | 0.85 | 11 | ||
rs4813802 | 0.776 | 0.080 | 20 | 6718948 | regulatory region variant | T/G | snv | 0.28 | 11 | ||
rs6063514 | 0.776 | 0.080 | 20 | 50438781 | intergenic variant | C/T | snv | 0.42 | 11 | ||
rs11087784 | 0.776 | 0.080 | 20 | 7760329 | intergenic variant | A/G | snv | 0.13 | 10 | ||
rs1741640 | 0.776 | 0.080 | 20 | 62357358 | intron variant | T/C | snv | 0.66 | 10 | ||
rs189583 | 0.776 | 0.080 | 20 | 6395810 | regulatory region variant | G/C;T | snv | 10 | |||
rs2423279 | 0.790 | 0.080 | 20 | 7831703 | downstream gene variant | T/C | snv | 0.29 | 10 | ||
rs2427308 | 0.790 | 0.080 | 20 | 62394395 | intron variant | C/T | snv | 0.22 | 10 | ||
rs28488 | 0.776 | 0.080 | 20 | 6781574 | downstream gene variant | C/T | snv | 0.68 | 10 | ||
rs6031311 | 0.776 | 0.080 | 20 | 44037835 | intron variant | C/T | snv | 0.73 | 10 | ||
rs6051080 | 0.790 | 0.080 | 20 | 25995038 | intron variant | A/G | snv | 0.48 | 10 | ||
rs6066825 | 0.776 | 0.080 | 20 | 48723580 | intron variant | A/G;T | snv | 10 | |||
rs6067417 | 0.776 | 0.080 | 20 | 50367160 | intergenic variant | C/T | snv | 0.33 | 10 |