Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10964862 | 9 | 21151554 | intergenic variant | C/A;G | snv | 1 | |||||
rs946486 | 9 | 130770618 | intron variant | C/T | snv | 0.44 | 1 | ||||
rs867748453 | 7 | 140781608 | missense variant | G/A | snv | 1 | |||||
rs353630 | 1.000 | 0.080 | 11 | 35166644 | intron variant | G/A | snv | 0.33 | 1 | ||
rs3206652 | 3 | 108046402 | 3 prime UTR variant | T/C | snv | 0.27 | 1 | ||||
rs3804639 | 3 | 108071988 | intron variant | G/T | snv | 0.28 | 1 | ||||
rs9879947 | 3 | 108046545 | 3 prime UTR variant | G/A | snv | 0.45 | 1 | ||||
rs684559 | 1 | 111215824 | intron variant | G/A | snv | 0.27 | 1 | ||||
rs1053129 | 5 | 80626901 | 3 prime UTR variant | C/A;T | snv | 1 | |||||
rs1472189 | 11 | 11962338 | 3 prime UTR variant | C/T | snv | 0.25 | 1 | ||||
rs7795743 | 7 | 55182437 | non coding transcript exon variant | G/A | snv | 0.56 | 1 | ||||
rs1131692237 | 1.000 | 0.040 | 17 | 39725161 | missense variant | T/G | snv | 1 | |||
rs10964859 | 9 | 21140673 | 3 prime UTR variant | C/A;G | snv | 1 | |||||
rs779724499 | 12 | 54411885 | missense variant | G/A | snv | 1 | |||||
rs200246209 | 11 | 102527789 | synonymous variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |||
rs2375801 | 4 | 186550471 | intron variant | T/C | snv | 0.34 | 1 | ||||
rs370006648 | 15 | 23687168 | missense variant | G/A | snv | 4.1E-05 | 7.0E-05 | 1 | |||
rs148626207 | 4 | 102612593 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | |||
rs71310379 | 3 | 179199003 | missense variant | C/A | snv | 4.4E-05 | 4.2E-05 | 1 | |||
rs756160717 | 3 | 12585204 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 1 | |||
rs2994809 | 1 | 119809354 | intron variant | T/C | snv | 0.91 | 1 | ||||
rs377767422 | 10 | 43119635 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |||
rs1317052311 | X | 15358134 | missense variant | C/A | snv | 5.5E-06 | 1 | ||||
rs6475526 | 1.000 | 0.080 | 9 | 21242162 | upstream gene variant | C/T | snv | 0.33 | 2 | ||
rs1340026226 | 1.000 | 0.080 | X | 67711662 | missense variant | G/A | snv | 9.5E-06 | 2 |