Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1429638 | 0.925 | 0.080 | 4 | 73872213 | downstream gene variant | C/A;G | snv | 0.17 | 2 | ||
rs1891320 | 0.925 | 0.080 | 1 | 19970618 | upstream gene variant | C/T | snv | 0.20 | 2 | ||
rs11684747 | 0.925 | 0.080 | 2 | 9557042 | upstream gene variant | A/G | snv | 0.19 | 2 | ||
rs11689958 | 0.925 | 0.080 | 2 | 9557277 | upstream gene variant | G/A | snv | 0.19 | 2 | ||
rs17602729 | 0.925 | 0.080 | 1 | 114693436 | stop gained | G/A;T | snv | 8.6E-02 | 2 | ||
rs11216153 | 0.925 | 0.080 | 11 | 116834384 | upstream gene variant | G/T | snv | 0.16 | 2 | ||
rs506027 | 0.925 | 0.080 | 6 | 106326589 | upstream gene variant | G/A | snv | 0.57 | 2 | ||
rs497116 | 0.925 | 0.080 | 11 | 104892390 | stop lost | A/G | snv | 4.3E-02 | 2 | ||
rs1915087 | 0.925 | 0.080 | 3 | 122119944 | 3 prime UTR variant | T/C | snv | 2 | |||
rs2332096 | 0.925 | 0.080 | 3 | 122102296 | intron variant | T/A;G | snv | 2 | |||
rs11666254 | 0.925 | 0.080 | 19 | 51759909 | intron variant | A/G | snv | 0.28 | 2 | ||
rs2808530 | 0.925 | 0.080 | 9 | 98576823 | intron variant | A/C | snv | 0.12 | 2 | ||
rs1419560997 | 0.925 | 0.080 | 11 | 117993410 | splice region variant | G/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs2715267 | 0.925 | 0.080 | 3 | 122052011 | upstream gene variant | G/A;T | snv | 2 | |||
rs41279766 | 0.925 | 0.080 | 2 | 118970217 | missense variant | C/G;T | snv | 2.1E-03 | 2 | ||
rs12605436 | 0.925 | 0.080 | 18 | 35906684 | upstream gene variant | C/T | snv | 9.1E-02 | 2 | ||
rs1153879 | 0.925 | 0.080 | 3 | 136392816 | intron variant | G/T | snv | 2 | |||
rs595209 | 0.925 | 0.080 | 11 | 126292326 | intron variant | A/C;G | snv | 2 | |||
rs8177375 | 0.925 | 0.080 | 11 | 126293169 | 3 prime UTR variant | A/G | snv | 0.12 | 0.13 | 2 | |
rs5744105 | 0.925 | 0.080 | 1 | 223142735 | intron variant | G/C | snv | 0.57 | 2 | ||
rs4755453 | 0.925 | 0.080 | 11 | 36509094 | intron variant | C/A;G;T | snv | 2 | |||
rs352162 | 0.882 | 0.160 | 3 | 52218953 | non coding transcript exon variant | T/C | snv | 0.55 | 3 | ||
rs7022797 | 0.882 | 0.120 | 9 | 88989548 | upstream gene variant | T/G | snv | 0.38 | 3 | ||
rs1475145065 | 0.882 | 0.080 | 14 | 24574706 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 3 | ||
rs2839693 | 0.882 | 0.120 | 10 | 44379119 | intron variant | T/A;C | snv | 3 |