Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3788533 | 0.925 | 0.040 | 22 | 38127239 | non coding transcript exon variant | C/G | snv | 0.47 | 3 | ||
rs12201676 | 0.925 | 0.040 | 6 | 89022382 | regulatory region variant | T/C | snv | 0.21 | 4 | ||
rs17746001 | 0.925 | 0.040 | 4 | 179734472 | intergenic variant | C/T | snv | 5.3E-02 | 4 | ||
rs2054399 | 0.925 | 0.040 | 3 | 178623794 | intron variant | G/A;C | snv | 4 | |||
rs4356203 | 0.925 | 0.040 | 11 | 17138601 | intron variant | A/G | snv | 0.31 | 4 | ||
rs7219021 | 0.925 | 0.040 | 17 | 48763179 | intron variant | T/G | snv | 0.26 | 4 | ||
rs7872515 | 0.925 | 0.040 | 9 | 92060258 | intron variant | G/A | snv | 0.25 | 4 | ||
rs802568 | 0.925 | 0.040 | 7 | 146262151 | intron variant | T/G | snv | 0.17 | 4 | ||
rs947267 | 0.882 | 0.040 | 13 | 105487313 | intron variant | T/G | snv | 0.51 | 4 | ||
rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 5 | ||
rs1039002 | 0.851 | 0.080 | 6 | 165741969 | intron variant | G/A;T | snv | 5 | |||
rs11789399 | 0.882 | 0.040 | 9 | 118597008 | intergenic variant | G/A;C | snv | 5 | |||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs2524005 | 0.882 | 0.160 | 6 | 29931900 | upstream gene variant | G/A | snv | 0.18 | 5 | ||
rs6465084 | 0.851 | 0.040 | 7 | 86774159 | intron variant | A/G | snv | 0.26 | 5 | ||
rs6484218 | 0.882 | 0.040 | 11 | 10369034 | intron variant | G/A | snv | 0.21 | 5 | ||
rs778294 | 0.851 | 0.040 | 13 | 105489886 | synonymous variant | C/A;T | snv | 0.27; 4.0E-06 | 0.26 | 5 | |
rs2239547 | 0.882 | 0.040 | 3 | 52821213 | intron variant | T/C | snv | 0.27 | 6 | ||
rs35753505 | 0.827 | 0.080 | 8 | 31616625 | intergenic variant | T/A;C | snv | 6 | |||
rs3803300 | 0.827 | 0.120 | 14 | 104803442 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 6 | |||
rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 7 | ||
rs12966547 | 0.827 | 0.040 | 18 | 55084786 | intergenic variant | G/A | snv | 0.39 | 7 | ||
rs2391191 | 0.807 | 0.080 | 13 | 105467097 | missense variant | G/A | snv | 0.40 | 0.32 | 7 | |
rs4650608 | 0.851 | 0.040 | 1 | 78772330 | intergenic variant | T/C | snv | 0.29 | 7 |