Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17277546 | 7 | 99891948 | 3 prime UTR variant | G/A | snv | 3.1E-02 | 4 | ||||
rs4481233 | 0.925 | 0.120 | 4 | 9954455 | intron variant | C/T | snv | 0.16 | 5 | ||
rs1447352 | 11 | 92989595 | downstream gene variant | G/A | snv | 0.55 | 2 | ||||
rs4905014 | 0.851 | 0.120 | 14 | 92945686 | intron variant | G/A;C | snv | 16 | |||
rs12579302 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 19 | ||
rs11185790 | 10 | 89612776 | intron variant | G/A | snv | 0.15 | 3 | ||||
rs494562 | 6 | 85407411 | intergenic variant | A/G | snv | 0.16 | 2 | ||||
rs8082812 | 0.851 | 0.120 | 18 | 8522684 | intergenic variant | C/A | snv | 4.6E-02 | 16 | ||
rs9942416 | 5 | 75741470 | intergenic variant | C/G | snv | 0.53 | 9 | ||||
rs211718 | 1 | 75640990 | downstream gene variant | T/C | snv | 0.75 | 3 | ||||
rs5744680 | 0.851 | 0.120 | 5 | 75584065 | intron variant | G/A | snv | 0.55 | 18 | ||
rs4704221 | 0.851 | 0.120 | 5 | 75463358 | intron variant | T/A;C | snv | 16 | |||
rs7703051 | 0.851 | 0.120 | 5 | 75329662 | intron variant | C/A | snv | 0.38 | 18 | ||
rs799165 | 0.851 | 0.120 | 7 | 73637727 | intergenic variant | T/A | snv | 0.13 | 17 | ||
rs13391552 | 2 | 73591809 | intron variant | G/A;C | snv | 2 | |||||
rs2074755 | 0.807 | 0.240 | 7 | 73462836 | non coding transcript exon variant | T/C | snv | 9.2E-02 | 20 | ||
rs7190256 | 0.851 | 0.120 | 16 | 72963084 | intron variant | C/T | snv | 0.94 | 16 | ||
rs6499165 | 16 | 68292297 | non coding transcript exon variant | A/C | snv | 0.80 | 2 | ||||
rs12753193 | 1 | 65703996 | non coding transcript exon variant | G/A | snv | 0.58 | 3 | ||||
rs4329 | 17 | 63486097 | intron variant | A/C;G | snv | 2 | |||||
rs2652822 | 15 | 63130573 | 3 prime UTR variant | T/C | snv | 0.41 | 2 | ||||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 33 | ||
rs7094971 | 0.925 | 0.120 | 10 | 59689806 | intron variant | A/G | snv | 0.13 | 4 | ||
rs261332 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 20 | ||
rs247617 | 0.827 | 0.160 | 16 | 56956804 | regulatory region variant | C/A | snv | 0.29 | 20 |