Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10061469 | 5 | 73222321 | intron variant | T/C | snv | 0.37 | 1 | ||||
rs10142466 | 14 | 68805067 | intergenic variant | A/C;G;T | snv | 1 | |||||
rs10521318 | 16 | 85977731 | intron variant | C/G;T | snv | 1 | |||||
rs11187157 | 10 | 92742487 | TF binding site variant | T/C | snv | 0.40 | 1 | ||||
rs11641016 | 16 | 85981275 | intron variant | C/G | snv | 0.18 | 1 | ||||
rs11677953 | 2 | 218256940 | non coding transcript exon variant | G/A | snv | 0.36 | 1 | ||||
rs12585310 | 13 | 26954210 | intergenic variant | G/A | snv | 0.27 | 1 | ||||
rs1388585 | 12 | 40137889 | downstream gene variant | G/A | snv | 0.95 | 1 | ||||
rs149169037 | 7 | 20537675 | intergenic variant | G/A | snv | 5.5E-02 | 1 | ||||
rs17000400 | 4 | 75251521 | regulatory region variant | C/T | snv | 0.12 | 1 | ||||
rs2427870 | X | 136581905 | upstream gene variant | C/T | snv | 0.52 | 1 | ||||
rs2472649 | 4 | 73991991 | upstream gene variant | A/G;T | snv | 1 | |||||
rs2839073 | 21 | 45953845 | regulatory region variant | T/C | snv | 0.16 | 1 | ||||
rs2847278 | 18 | 12778716 | upstream gene variant | C/T | snv | 0.83 | 1 | ||||
rs4836519 | 5 | 130681594 | intron variant | T/A;C | snv | 1 | |||||
rs4899554 | 14 | 75234518 | downstream gene variant | C/T | snv | 0.14 | 1 | ||||
rs6935723 | 6 | 32713892 | upstream gene variant | T/C | snv | 0.29 | 1 | ||||
rs72634258 | 1 | 8090578 | intron variant | T/C | snv | 0.13 | 1 | ||||
rs7547569 | 1 | 67265685 | downstream gene variant | T/C | snv | 4.7E-02 | 1 | ||||
rs7911264 | 10 | 92677094 | intergenic variant | T/A;C;G | snv | 1 | |||||
rs7968307 | 12 | 114620647 | upstream gene variant | T/C | snv | 0.33 | 1 | ||||
rs8009169 | 14 | 42813211 | intergenic variant | G/C | snv | 0.78 | 1 | ||||
rs9313808 | 5 | 159393836 | intron variant | A/G | snv | 0.89 | 1 | ||||
rs950318 | 3 | 80354036 | intergenic variant | C/G | snv | 0.22 | 1 | ||||
rs6545800 | 2 | 24896016 | intron variant | C/T | snv | 0.53 | 1 |