Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs754388 | 0.882 | 0.120 | 14 | 92649065 | intron variant | G/C;T | snv | 5 | |||
rs7655625 | 1.000 | 0.040 | 4 | 144564763 | intron variant | T/C;G | snv | 5 | |||
rs2955083 | 1.000 | 0.040 | 3 | 128242335 | intron variant | T/A | snv | 0.89 | 4 | ||
rs8756 | 0.882 | 0.200 | 12 | 65965972 | 3 prime UTR variant | C/A | snv | 0.56 | 4 | ||
rs3791979 | 1.000 | 0.040 | 2 | 217802649 | 3 prime UTR variant | T/A;C;G | snv | 3 | |||
rs57942103 | 1.000 | 0.040 | 8 | 105501233 | intron variant | A/C | snv | 0.25 | 3 | ||
rs10883944 | 1.000 | 0.040 | 10 | 103891899 | intron variant | G/T | snv | 0.31 | 2 | ||
rs1158317 | 1.000 | 0.040 | 6 | 120626545 | intron variant | C/T | snv | 0.58 | 2 | ||
rs12173787 | 1.000 | 0.040 | 6 | 33767694 | downstream gene variant | G/C | snv | 0.51 | 2 | ||
rs12709669 | 1.000 | 0.040 | 18 | 22227108 | intron variant | T/G | snv | 0.56 | 2 | ||
rs13409705 | 1.000 | 0.040 | 2 | 28613010 | intron variant | C/G | snv | 0.15 | 2 | ||
rs17186681 | 1.000 | 0.040 | 15 | 63696566 | intron variant | A/T | snv | 0.16 | 2 | ||
rs17431820 | 1.000 | 0.040 | 16 | 65094555 | intron variant | T/G | snv | 7.3E-02 | 2 | ||
rs2512519 | 1.000 | 0.040 | 11 | 78241969 | intron variant | C/T | snv | 0.18 | 2 | ||
rs3738676 | 1.000 | 0.040 | 1 | 39525916 | 3 prime UTR variant | G/A;T | snv | 2 | |||
rs4746139 | 1.000 | 0.040 | 10 | 73647891 | synonymous variant | A/C | snv | 0.16 | 0.14 | 2 | |
rs56386186 | 1.000 | 0.040 | 14 | 102193651 | intron variant | T/C | snv | 9.7E-02 | 2 | ||
rs59985166 | 1.000 | 0.040 | 1 | 10662447 | intron variant | C/T | snv | 4.9E-02 | 2 | ||
rs7143026 | 1.000 | 0.040 | 14 | 65784238 | intergenic variant | A/G | snv | 0.38 | 2 | ||
rs7449334 | 1.000 | 0.040 | 5 | 91046595 | intron variant | G/A;C | snv | 0.76 | 2 | ||
rs9859058 | 1.000 | 0.040 | 3 | 156795028 | intron variant | C/A | snv | 0.39 | 2 |