Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3731211 | 9 | 21986848 | intron variant | T/A | snv | 0.74 | 7 | ||||
rs2524079 | 6 | 31274397 | intron variant | G/A | snv | 0.44 | 6 | ||||
rs3735485 | 7 | 44969742 | missense variant | A/G | snv | 0.87 | 0.88 | 6 | |||
rs4737010 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 6 | ||||
rs6475611 | 9 | 22151140 | intergenic variant | G/A | snv | 0.21 | 6 | ||||
rs13063578 | 3 | 47046347 | intron variant | T/A | snv | 0.46 | 5 | ||||
rs142550358 | 9 | 88777772 | intron variant | CT/- | delins | 3.9E-02 | 5 | ||||
rs5754100 | 0.882 | 22 | 21561877 | intron variant | T/C | snv | 0.18 | 5 | |||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs34338164 | 2 | 68388414 | missense variant | A/C | snv | 8.0E-03 | 7.8E-03 | 4 | |||
rs3812049 | 5 | 128083158 | non coding transcript exon variant | C/A;G;T | snv | 4 | |||||
rs10466905 | 12 | 6393666 | upstream gene variant | G/A | snv | 0.21 | 3 | ||||
rs13092376 | 3 | 196789417 | intron variant | A/C;G | snv | 0.33 | 3 | ||||
rs149290349 | 2 | 43224818 | missense variant | G/A;T | snv | 6.7E-02 | 3 | ||||
rs28577594 | 12 | 123411359 | 3 prime UTR variant | G/C | snv | 0.56 | 3 | ||||
rs36084354 | 19 | 1079960 | missense variant | G/A | snv | 5.7E-02 | 5.9E-02 | 3 | |||
rs61387190 | 19 | 43756777 | upstream gene variant | C/A;T | snv | 3 | |||||
rs62237617 | 22 | 28365160 | intron variant | C/G;T | snv | 1.9E-03 | 3 | ||||
rs748113 | 10 | 71749034 | 3 prime UTR variant | T/C | snv | 0.38 | 3 | ||||
rs79716587 | 2 | 143129250 | intron variant | G/A | snv | 7.9E-02 | 3 | ||||
rs9494142 | 6 | 135110502 | TF binding site variant | T/C | snv | 0.21 | 3 | ||||
rs10087240 | 8 | 128000328 | intron variant | C/G;T | snv | 2 | |||||
rs10422126 | 19 | 13837498 | non coding transcript exon variant | G/A | snv | 0.37 | 2 | ||||
rs1285886 | 6 | 7140598 | intron variant | G/A | snv | 0.28 | 2 | ||||
rs17041439 | 12 | 101479462 | intron variant | A/C | snv | 7.0E-02 | 2 |