Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10006235 | 1.000 | 0.040 | 4 | 129748953 | non coding transcript exon variant | T/C | snv | 0.73 | 2 | ||
rs10010325 | 1.000 | 0.040 | 4 | 105185196 | intron variant | C/A;G;T | snv | 3 | |||
rs10011007 | 4 | 130143535 | intergenic variant | A/C | snv | 8.3E-02 | 1 | ||||
rs10031823 | 4 | 102203874 | intergenic variant | T/C | snv | 0.68 | 1 | ||||
rs1003531 | 19 | 2206576 | intron variant | G/T | snv | 0.21 | 1 | ||||
rs10044158 | 5 | 63666886 | intergenic variant | G/A | snv | 0.55 | 1 | ||||
rs10061788 | 1.000 | 0.040 | 5 | 88638889 | intron variant | G/A;T | snv | 2 | |||
rs10070734 | 5 | 88644208 | intron variant | T/A;C | snv | 1 | |||||
rs1007934 | 14 | 72996771 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs1008078 | 1.000 | 0.040 | 1 | 90724174 | non coding transcript exon variant | C/T | snv | 0.33 | 2 | ||
rs10119 | 0.925 | 0.080 | 19 | 44903416 | 3 prime UTR variant | G/A | snv | 0.28 | 1 | ||
rs10129426 | 14 | 103552118 | upstream gene variant | G/A | snv | 0.54 | 2 | ||||
rs10133551 | 14 | 32813026 | intron variant | T/C | snv | 0.30 | 1 | ||||
rs10145335 | 14 | 98081411 | intron variant | G/A | snv | 0.21 | 1 | ||||
rs10147849 | 14 | 32835225 | 3 prime UTR variant | T/C | snv | 0.46 | 1 | ||||
rs10149470 | 1.000 | 0.040 | 14 | 103551616 | upstream gene variant | A/G | snv | 0.54 | 3 | ||
rs10165862 | 2 | 73383615 | intron variant | C/T | snv | 0.45 | 1 | ||||
rs10175405 | 2 | 100703250 | regulatory region variant | G/T | snv | 0.33 | 1 | ||||
rs10182272 | 2 | 165677305 | intron variant | G/A | snv | 0.24 | 1 | ||||
rs10185725 | 2 | 154607197 | intergenic variant | C/T | snv | 0.35 | 1 | ||||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 5 | ||
rs10189912 | 2 | 143405040 | intron variant | A/G | snv | 0.27 | 1 | ||||
rs10191758 | 2 | 143505711 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs10192369 | 2 | 160524377 | intergenic variant | G/A | snv | 0.45 | 2 | ||||
rs10193972 | 2 | 73490529 | missense variant | A/G | snv | 0.26 | 0.39 | 1 |