Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10019888 | 4 | 26061368 | regulatory region variant | A/G | snv | 0.17 | 2 | ||||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 1 | ||||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 3 | ||
rs1020731 | 1.000 | 0.080 | 2 | 160287544 | intron variant | G/A | snv | 0.69 | 1 | ||
rs1034207 | 6 | 127016554 | intron variant | C/A;G;T | snv | 0.94 | 1 | ||||
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 6 | ||
rs1055144 | 1.000 | 0.040 | 7 | 25831489 | non coding transcript exon variant | C/T | snv | 0.16 | 2 | ||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 4 | ||||
rs10894604 | 11 | 132771851 | non coding transcript exon variant | T/G | snv | 0.26 | 1 | ||||
rs11075985 | 1.000 | 0.080 | 16 | 53771295 | intron variant | C/A | snv | 0.42 | 2 | ||
rs11102800 | 1.000 | 0.040 | 1 | 114498310 | intron variant | C/T | snv | 0.58 | 1 | ||
rs11154370 | 6 | 126846446 | intron variant | A/G;T | snv | 1 | |||||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 9 | |||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 1 | |||
rs11724804 | 0.882 | 0.160 | 4 | 971991 | intron variant | G/A | snv | 0.43 | 1 | ||
rs11897119 | 2 | 66544868 | intron variant | T/A;C | snv | 1 | |||||
rs12061508 | 1.000 | 0.040 | 1 | 196615338 | intergenic variant | G/A | snv | 0.23 | 2 | ||
rs12110693 | 6 | 121837124 | intergenic variant | G/A | snv | 0.23 | 1 | ||||
rs12440667 | 1.000 | 0.040 | 15 | 73939098 | intron variant | C/A;T | snv | 1 | |||
rs12440695 | 15 | 62142957 | regulatory region variant | T/C | snv | 0.32 | 2 | ||||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 1 | |||
rs1254319 | 1.000 | 14 | 60437039 | missense variant | G/A | snv | 0.35 | 0.36 | 1 | ||
rs12714415 | 2 | 651430 | intergenic variant | T/C | snv | 0.19 | 2 | ||||
rs12731740 | 1 | 207851475 | intron variant | C/T | snv | 9.1E-02 | 1 | ||||
rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 3 |