Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10801558 | 1.000 | 0.040 | 1 | 196729914 | intron variant | T/G | snv | 0.46 | 2 | ||
rs10801559 | 1.000 | 0.040 | 1 | 196735074 | intron variant | G/A | snv | 0.44 | 2 | ||
rs10922104 | 1.000 | 0.040 | 1 | 196718600 | intron variant | A/C;G | snv | 2 | |||
rs10922105 | 1.000 | 0.040 | 1 | 196721120 | intron variant | A/C;T | snv | 2 | |||
rs10922108 | 1.000 | 0.040 | 1 | 196732343 | intron variant | A/T | snv | 0.46 | 2 | ||
rs11118892 | 1.000 | 0.040 | 1 | 221910253 | intron variant | G/C;T | snv | 2 | |||
rs114931935 | 0.925 | 0.080 | 1 | 161690011 | upstream gene variant | G/A | snv | 3.0E-02 | 2 | ||
rs1329427 | 1.000 | 0.040 | 1 | 196735429 | intron variant | C/T | snv | 0.44 | 2 | ||
rs143262451 | 1.000 | 0.040 | 1 | 93407898 | intergenic variant | G/A | snv | 2.6E-03 | 2 | ||
rs144177292 | 1.000 | 0.040 | 1 | 201994931 | intron variant | C/T | snv | 2.8E-03 | 2 | ||
rs181020201 | 1.000 | 0.040 | 1 | 51134390 | intron variant | A/C | snv | 1.1E-04 | 2 | ||
rs3009947 | 1.000 | 0.040 | 1 | 218515813 | intron variant | T/C | snv | 0.47 | 2 | ||
rs305221 | 1.000 | 0.040 | 1 | 88733302 | intron variant | G/A | snv | 0.59 | 2 | ||
rs34585985 | 0.925 | 0.080 | 1 | 210316066 | intergenic variant | A/G | snv | 5.2E-02 | 2 | ||
rs3738676 | 1.000 | 0.040 | 1 | 39525916 | 3 prime UTR variant | G/A;T | snv | 2 | |||
rs3766405 | 1.000 | 0.040 | 1 | 196726031 | intron variant | C/T | snv | 0.46 | 2 | ||
rs3831317 | 0.925 | 0.080 | 1 | 203217822 | stop gained | -/AGACCATGGCCCCGCCCAGTCCCT | delins | 2 | |||
rs3924223 | 1.000 | 0.040 | 1 | 221905852 | intron variant | G/A;C | snv | 2 | |||
rs4457591 | 1.000 | 0.040 | 1 | 221905258 | intron variant | T/C | snv | 0.48 | 2 | ||
rs59985166 | 1.000 | 0.040 | 1 | 10662447 | intron variant | C/T | snv | 4.9E-02 | 2 | ||
rs61781370 | 1.000 | 0.040 | 1 | 39579628 | upstream gene variant | A/C | snv | 0.17 | 2 | ||
rs6677089 | 1.000 | 0.040 | 1 | 196715183 | intron variant | A/C | snv | 0.46 | 2 | ||
rs6688272 | 1.000 | 0.040 | 1 | 196715262 | intron variant | G/T | snv | 0.44 | 2 | ||
rs7514261 | 1.000 | 0.040 | 1 | 196731784 | intron variant | G/A;T | snv | 2 | |||
rs10890311 | 1.000 | 0.040 | 1 | 44602096 | intron variant | C/T | snv | 0.22 | 1 |