Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs59876823 | 13 | 100082270 | intron variant | C/A | snv | 0.10 | 2 | ||||
rs12588659 | 14 | 100121476 | intron variant | C/A | snv | 6.6E-02 | 1 | ||||
rs10958852 | 9 | 10060843 | intron variant | C/T | snv | 4.5E-04 | 2 | ||||
rs182466621 | 2 | 100730839 | intergenic variant | G/A;T | snv | 2 | |||||
rs140386998 | X | 100959983 | downstream gene variant | C/T | snv | 3.7E-02 | 2 | ||||
rs60866311 | 2 | 100975599 | non coding transcript exon variant | T/G | snv | 4.1E-02 | 7.2E-02 | 2 | |||
rs17396340 | 1 | 10226118 | intron variant | G/A;C | snv | 3 | |||||
rs3862030 | 10 | 102567827 | intron variant | A/G | snv | 0.45 | 2 | ||||
rs7917772 | 10 | 102727686 | 3 prime UTR variant | G/A;C | snv | 0.46 | 3 | ||||
rs71417845 | 14 | 103210903 | downstream gene variant | C/G | snv | 1.7E-02 | 2 | ||||
rs41427747 | 4 | 103999322 | intron variant | G/T | snv | 5.6E-02 | 2 | ||||
rs395962 | 6 | 104949543 | intron variant | T/G | snv | 0.72 | 6 | ||||
rs10991437 | 9 | 104973639 | intron variant | C/A | snv | 9.0E-02 | 2 | ||||
rs58376408 | 16 | 10504450 | regulatory region variant | C/G | snv | 6.5E-02 | 2 | ||||
rs144529734 | 10 | 105647558 | intergenic variant | G/T | snv | 1.4E-02 | 2 | ||||
rs9408815 | 9 | 106128240 | intron variant | C/G | snv | 0.20 | 2 | ||||
rs9409082 | 9 | 106138768 | intron variant | C/T | snv | 0.20 | 2 | ||||
rs670752 | 3 | 107594133 | intron variant | G/A;T | snv | 2 | |||||
rs13271456 | 8 | 10767736 | intron variant | G/A | snv | 2.7E-02 | 2 | ||||
rs6437740 | 3 | 107746970 | intron variant | T/C | snv | 0.25 | 2 | ||||
rs12710258 | 19 | 10879653 | intron variant | C/T | snv | 0.16 | 2 | ||||
rs10041657 | 5 | 108816727 | intron variant | G/A | snv | 0.23 | 2 | ||||
rs78553789 | 13 | 108904171 | intron variant | T/C | snv | 2.3E-02 | 2 | ||||
rs848353 | 1.000 | 0.080 | 7 | 108908603 | upstream gene variant | A/G | snv | 0.14 | 3 | ||
rs117178387 | 6 | 110815877 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 2 |