Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11790959 | 1.000 | 0.080 | 9 | 134127023 | intergenic variant | C/A;T | snv | 3.4E-03 | 1 | ||
rs17028719 | 1.000 | 0.080 | 1 | 5734948 | intergenic variant | A/G | snv | 4.8E-02 | 1 | ||
rs17616845 | 1.000 | 0.080 | 7 | 12741918 | intron variant | T/C | snv | 0.15 | 1 | ||
rs1912461 | 1.000 | 0.080 | 15 | 36052338 | intron variant | T/C | snv | 3.3E-02 | 1 | ||
rs1943418 | 1.000 | 0.080 | 18 | 59812296 | intergenic variant | T/C | snv | 0.76 | 1 | ||
rs1995364 | 1.000 | 0.080 | 5 | 10903669 | intergenic variant | A/G | snv | 0.62 | 1 | ||
rs4384980 | 1.000 | 0.080 | 3 | 182741281 | upstream gene variant | A/C | snv | 0.48 | 1 | ||
rs4610908 | 1.000 | 0.080 | X | 35166418 | intergenic variant | G/A | snv | 0.24 | 1 | ||
rs567926 | 1.000 | 0.080 | 4 | 46239752 | downstream gene variant | G/A | snv | 0.63 | 1 | ||
rs5916144 | 1.000 | 0.080 | X | 5561570 | intergenic variant | C/A;G | snv | 1 | |||
rs5961794 | 1.000 | 0.080 | X | 5656287 | intron variant | A/G | snv | 0.27 | 1 | ||
rs602618 | 1.000 | 0.080 | 10 | 111083327 | downstream gene variant | C/A | snv | 0.58 | 1 | ||
rs6425323 | 1.000 | 0.080 | 1 | 175155900 | downstream gene variant | C/T | snv | 0.39 | 1 | ||
rs7597960 | 1.000 | 0.080 | 2 | 122667075 | intron variant | A/G;T | snv | 1 | |||
rs7607774 | 1.000 | 0.080 | 2 | 236520511 | intergenic variant | G/A | snv | 7.4E-02 | 1 | ||
rs7777391 | 1.000 | 0.080 | 7 | 117981823 | intergenic variant | A/G | snv | 0.60 | 1 | ||
rs9847462 | 1.000 | 0.080 | 3 | 164840807 | intergenic variant | A/G | snv | 0.14 | 1 | ||
rs994029 | 1.000 | 0.080 | 9 | 86760399 | downstream gene variant | C/T | snv | 0.71 | 1 | ||
rs727532 | 1.000 | 0.080 | 10 | 114445017 | intron variant | A/G | snv | 0.17 | 1 | ||
rs12006002 | 1.000 | 0.080 | 9 | 18166901 | intron variant | C/T | snv | 0.30 | 1 | ||
rs4147541 | 1.000 | 0.080 | 4 | 99353000 | upstream gene variant | G/C | snv | 0.33 | 1 | ||
rs1042364 | 1.000 | 0.080 | 4 | 99124423 | stop gained | T/A;C | snv | 0.78 | 1 | ||
rs2303317 | 1.000 | 0.080 | 9 | 72927026 | non coding transcript exon variant | G/A;T | snv | 1 | |||
rs63319 | 1.000 | 0.080 | 9 | 72909868 | intron variant | G/T | snv | 0.56 | 1 | ||
rs142427338 | 1.000 | 0.080 | 9 | 38396880 | stop gained | C/T | snv | 1.0E-03; 4.0E-06 | 1.0E-03 | 1 |