Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 9 | ||||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 | |||||
rs643434 | 9 | 133266942 | intron variant | A/G;T | snv | 8 | |||||
rs674302 | 9 | 133271249 | intron variant | A/T | snv | 8 | |||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 7 | ||||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs12679834 | 8 | 19962922 | intron variant | T/C | snv | 9.4E-02 | 7 | ||||
rs174529 | 11 | 61776489 | intron variant | T/C | snv | 0.34 | 7 | ||||
rs1875263 | 1.000 | 2 | 233716976 | intron variant | C/G;T | snv | 7 | ||||
rs644234 | 9 | 133266804 | intron variant | G/T | snv | 7 | |||||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 7 | ||||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 7 | |||||
rs10173355 | 1.000 | 2 | 233688675 | intron variant | A/G;T | snv | 6 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 6 | |||
rs11207997 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 6 | ||||
rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 6 | ||||
rs12720922 | 16 | 56966973 | intron variant | G/A | snv | 0.23 | 6 | ||||
rs2131925 | 1 | 62560271 | intron variant | G/T | snv | 0.57 | 6 | ||||
rs217181 | 16 | 72080103 | intron variant | C/T | snv | 0.20 | 6 | ||||
rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 6 | ||||
rs2741012 | 1.000 | 2 | 233600317 | upstream gene variant | C/T | snv | 0.24 | 6 | |||
rs4665710 | 2 | 20998163 | downstream gene variant | A/C | snv | 0.76 | 6 | ||||
rs583104 | 1 | 109278685 | downstream gene variant | G/T | snv | 0.63 | 6 |