Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10910476 | 1 | 234599210 | regulatory region variant | C/A;T | snv | 2 | |||||
rs11211480 | 1 | 47227548 | non coding transcript exon variant | A/G | snv | 0.42 | 4 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 7 | ||
rs2072671 | 0.752 | 0.280 | 1 | 20589208 | missense variant | A/C | snv | 0.28 | 0.25 | 16 | |
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs646179 | 1 | 62437203 | 5 prime UTR variant | A/G;T | snv | 2 | |||||
rs78024727 | 1 | 198580649 | intergenic variant | G/A | snv | 3.5E-02 | 2 | ||||
rs10197140 | 2 | 110852366 | intron variant | T/C | snv | 0.28 | 3 | ||||
rs112257498 | 2 | 189568259 | intron variant | C/G;T | snv | 2 | |||||
rs11683361 | 2 | 111622982 | intron variant | C/G | snv | 0.70 | 2 | ||||
rs143326447 | 0.925 | 0.080 | 2 | 111511155 | intron variant | T/C | snv | 0.11 | 4 | ||
rs2137283 | 2 | 60385322 | non coding transcript exon variant | C/A | snv | 0.30 | 4 | ||||
rs2139376 | 2 | 111385836 | intron variant | T/C | snv | 0.44 | 2 | ||||
rs2556097 | 2 | 159830550 | intron variant | C/A;T | snv | 2 | |||||
rs2661794 | 2 | 65412409 | intron variant | C/A;T | snv | 2 | |||||
rs4663199 | 2 | 235459395 | regulatory region variant | T/A | snv | 0.35 | 2 | ||||
rs4669306 | 2 | 8614076 | intron variant | G/A | snv | 0.51 | 2 | ||||
rs5831579 | 2 | 60402304 | intron variant | ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC | delins | 3 | |||||
rs60237566 | 2 | 230877996 | intron variant | T/G | snv | 0.21 | 0.25 | 2 | |||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs72803397 | 2 | 62303123 | intergenic variant | G/A | snv | 0.15 | 2 | ||||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs920112 | 2 | 173354407 | intron variant | G/A | snv | 1.0E-01 | 5 |