Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs142529006 | 7 | 100022093 | intron variant | T/A | snv | 6.9E-03 | 4 | ||||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 10 | ||
rs7384878 | 7 | 100334426 | intron variant | C/T | snv | 0.72 | 2 | ||||
rs72996119 | 11 | 100587081 | intergenic variant | A/G | snv | 7.8E-02 | 2 | ||||
rs41295942 | 7 | 100621008 | missense variant | C/T | snv | 2.0E-02 | 2.2E-02 | 2 | |||
rs717662 | 11 | 100623264 | intergenic variant | C/T | snv | 8.5E-02 | 2 | ||||
rs139178017 | 7 | 100628224 | splice region variant | C/T | snv | 3.1E-03 | 2.8E-03 | 2 | |||
rs9801017 | 7 | 100638579 | intron variant | G/A | snv | 0.65 | 3 | ||||
rs531909210 | 7 | 100641799 | intron variant | G/A | snv | 2.8E-03 | 3 | ||||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs73003836 | 11 | 100713940 | intron variant | C/T | snv | 7.0E-02 | 2 | ||||
rs7797559 | 7 | 101065852 | intergenic variant | A/C;G;T | snv | 2 | |||||
rs4615960 | 10 | 101438198 | intron variant | G/A | snv | 0.26 | 2 | ||||
rs67806247 | 19 | 1014539 | intron variant | TGATGGGGCG/-;TGATGGGGCGTGATGGGGCG | delins | 2 | |||||
rs636089 | 8 | 102065562 | intron variant | T/C | snv | 0.28 | 2 | ||||
rs57236717 | 14 | 102148541 | intron variant | AAA/-;A;AA;AAAA;AAAAA;AAAAAA;AAAAAAAAAA | delins | 2 | |||||
rs12883091 | 14 | 102202685 | intron variant | G/A | snv | 0.27 | 2 | ||||
rs3087686 | 14 | 102229226 | 3 prime UTR variant | A/G | snv | 0.33 | 2 | ||||
rs7692921 | 4 | 102326283 | intron variant | C/A | snv | 0.13 | 2 | ||||
rs368447685 | 5 | 1025534 | intron variant | T/C | snv | 1.3E-03 | 2 | ||||
rs4772494 | 13 | 102603946 | intron variant | A/G | snv | 0.65 | 2 | ||||
rs1190335 | 14 | 102645021 | intron variant | T/C;G | snv | 2 | |||||
rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
rs559546873 | 10 | 103186913 | intron variant | AAAA/-;A;AA;AAA;AAAAA;AAAAAA | delins | 0.33 | 2 | ||||
rs17616464 | 14 | 103373661 | downstream gene variant | C/G | snv | 6.5E-02 | 2 |