Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 4 | |||
rs10244051 | 1.000 | 0.080 | 7 | 15024208 | intergenic variant | T/A;G | snv | 3 | |||
rs13266634 | 0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 | 3 | ||
rs2066938 | 12 | 120722812 | 3 prime UTR variant | A/C;G | snv | 3 | |||||
rs2794520 | 0.807 | 0.240 | 1 | 159709026 | upstream gene variant | C/A;T | snv | 3 | |||
rs765547 | 0.827 | 0.160 | 8 | 20008763 | intergenic variant | G/A;C;T | snv | 3 | |||
rs13391552 | 2 | 73591809 | intron variant | G/A;C | snv | 2 | |||||
rs1495743 | 8 | 18415790 | intergenic variant | G/A;C | snv | 2 | |||||
rs1728918 | 0.827 | 0.160 | 2 | 27412596 | upstream gene variant | A/G;T | snv | 2 | |||
rs2403254 | 11 | 18303599 | intron variant | C/G;T | snv | 2 | |||||
rs2518049 | 10 | 5095844 | intron variant | A/G;T | snv | 2 | |||||
rs4329 | 17 | 63486097 | intron variant | A/C;G | snv | 2 | |||||
rs478442 | 0.851 | 0.120 | 2 | 21176344 | intergenic variant | G/C;T | snv | 2 | |||
rs17277546 | 7 | 99891948 | 3 prime UTR variant | G/A | snv | 3.1E-02 | 3 | ||||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 6 | ||
rs2023634 | 22 | 18984937 | intron variant | A/G | snv | 7.9E-02 | 2 | ||||
rs2074755 | 0.807 | 0.240 | 7 | 73462836 | non coding transcript exon variant | T/C | snv | 9.2E-02 | 4 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 6 | ||
rs799165 | 0.851 | 0.120 | 7 | 73637727 | intergenic variant | T/A | snv | 0.13 | 2 | ||
rs7094971 | 0.925 | 0.120 | 10 | 59689806 | intron variant | A/G | snv | 0.13 | 4 | ||
rs662138 | 6 | 160143444 | intron variant | C/G | snv | 0.14 | 2 | ||||
rs6975024 | 7 | 44192287 | intron variant | T/C | snv | 0.14 | 2 |