Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs11072567 | 15 | 76006403 | intron variant | A/G | snv | 0.43 | 5 | ||||
rs62033406 | 16 | 53790314 | intron variant | A/G | snv | 0.33 | 5 | ||||
rs79598313 | 1 | 26958422 | intron variant | C/A;T | snv | 5 | |||||
rs11204682 | 1 | 150623061 | intron variant | G/A;T | snv | 4 | |||||
rs11663816 | 18 | 60208994 | intergenic variant | T/C | snv | 0.20 | 4 | ||||
rs1407040 | 20 | 58897119 | intron variant | C/T | snv | 0.70 | 4 | ||||
rs2453580 | 17 | 19535008 | non coding transcript exon variant | T/C | snv | 0.37 | 4 | ||||
rs6026578 | 20 | 58888417 | 5 prime UTR variant | C/G | snv | 0.60 | 4 | ||||
rs60808706 | 11 | 2836003 | intron variant | G/A | snv | 0.12 | 4 | ||||
rs7752448 | 6 | 28333322 | intron variant | A/G | snv | 0.15 | 4 | ||||
rs9302635 | 16 | 72110275 | intron variant | T/C;G | snv | 4 | |||||
rs11940694 | 4 | 39413373 | intron variant | A/G | snv | 0.57 | 3 | ||||
rs143193096 | 15 | 98916098 | missense variant | G/A;C | snv | 8.4E-05; 4.0E-06 | 3 | ||||
rs151134704 | 4 | 102616435 | splice region variant | C/T | snv | 1.6E-04 | 9.1E-05 | 3 | |||
rs16856823 | 2 | 169343942 | intron variant | A/T | snv | 4.6E-02 | 3 | ||||
rs199592697 | 3 | 13854632 | missense variant | C/T | snv | 1.7E-04 | 1.1E-04 | 3 | |||
rs2867112 | 2 | 651349 | intergenic variant | T/G | snv | 0.18 | 3 | ||||
rs35506085 | 11 | 2144346 | intron variant | G/A | snv | 0.17 | 3 | ||||
rs4686914 | 3 | 187999752 | intron variant | C/T | snv | 0.27 | 3 | ||||
rs4788815 | 16 | 71600908 | intergenic variant | A/T | snv | 0.69 | 3 | ||||
rs78946096 | 3 | 132469319 | intron variant | A/G | snv | 3.8E-02 | 3 | ||||
rs11084786 | 19 | 34791277 | intron variant | A/G | snv | 0.38 | 2 | ||||
rs12134456 | 1 | 155752715 | intron variant | C/G | snv | 0.26 | 2 |