Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17168486 | 1.000 | 0.080 | 7 | 14858657 | intron variant | C/T | snv | 0.18 | 3 | ||
rs17277546 | 7 | 99891948 | 3 prime UTR variant | G/A | snv | 3.1E-02 | 3 | ||||
rs2066938 | 12 | 120722812 | 3 prime UTR variant | A/C;G | snv | 3 | |||||
rs211718 | 1 | 75640990 | downstream gene variant | T/C | snv | 0.75 | 3 | ||||
rs2794520 | 0.807 | 0.240 | 1 | 159709026 | upstream gene variant | C/A;T | snv | 3 | |||
rs4253252 | 4 | 186236304 | intron variant | T/G | snv | 0.56 | 3 | ||||
rs765547 | 0.827 | 0.160 | 8 | 20008763 | intergenic variant | G/A;C;T | snv | 3 | |||
rs7703051 | 0.851 | 0.120 | 5 | 75329662 | intron variant | C/A | snv | 0.38 | 3 | ||
rs7760535 | 6 | 111425880 | intron variant | G/C | snv | 0.46 | 3 | ||||
rs8396 | 4 | 158709665 | 3 prime UTR variant | T/C | snv | 0.29 | 3 | ||||
rs9393903 | 6 | 11042676 | intron variant | G/A | snv | 0.18 | 3 | ||||
rs10518693 | 15 | 40407823 | intron variant | C/T | snv | 0.37 | 2 | ||||
rs10799701 | 1 | 21494497 | intergenic variant | A/G | snv | 0.47 | 2 | ||||
rs11185790 | 10 | 89612776 | intron variant | G/A | snv | 0.15 | 2 | ||||
rs12670403 | 7 | 17269655 | intron variant | C/A | snv | 0.46 | 2 | ||||
rs12753193 | 1 | 65703996 | non coding transcript exon variant | G/A | snv | 0.58 | 2 | ||||
rs13391552 | 2 | 73591809 | intron variant | G/A;C | snv | 2 | |||||
rs1447352 | 11 | 92989595 | downstream gene variant | G/A | snv | 0.55 | 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 | |||
rs2023634 | 22 | 18984937 | intron variant | A/G | snv | 7.9E-02 | 2 | ||||
rs2087160 | 4 | 110413574 | intron variant | G/T | snv | 0.68 | 2 | ||||
rs2216405 | 2 | 210752170 | intergenic variant | A/G | snv | 0.15 | 2 | ||||
rs2403254 | 11 | 18303599 | intron variant | C/G;T | snv | 2 | |||||
rs2518049 | 10 | 5095844 | intron variant | A/G;T | snv | 2 |