Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 13 | ||
rs2246490 | 14 | 103517957 | downstream gene variant | G/T | snv | 0.67 | 1 | ||||
rs11826048 | 11 | 103527569 | intergenic variant | C/T | snv | 9.6E-02 | 1 | ||||
rs11111839 | 12 | 103916945 | intron variant | C/A | snv | 7.9E-02 | 1 | ||||
rs4387287 | 10 | 103918139 | 5 prime UTR variant | A/C | snv | 0.69 | 4 | ||||
rs144588452 | 9 | 104784371 | missense variant | C/T | snv | 2.2E-04 | 1.5E-04 | 1 | |||
rs2066718 | 0.882 | 0.120 | 9 | 104826974 | missense variant | C/G;T | snv | 4.3E-04; 5.4E-02 | 7 | ||
rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
rs145158522 | 10 | 104870101 | intron variant | C/A;G;T | snv | 1 | |||||
rs35783704 | 8 | 104954030 | intron variant | G/A | snv | 7.2E-02 | 2 | ||||
rs56388530 | 4 | 105989801 | intron variant | C/A;T | snv | 2 | |||||
rs17477177 | 1.000 | 0.080 | 7 | 106771412 | upstream gene variant | T/C | snv | 0.17 | 4 | ||
rs373644334 | 7 | 106867748 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 4.0E-06 | 1 | ||||
rs4754196 | 11 | 107226051 | intergenic variant | A/G | snv | 0.39 | 1 | ||||
rs880315 | 0.925 | 0.120 | 1 | 10736809 | intron variant | T/C | snv | 0.32 | 9 | ||
rs12212067 | 0.716 | 0.320 | 6 | 108659993 | intron variant | T/G | snv | 0.14 | 20 | ||
rs3087456 | 0.742 | 0.480 | 16 | 10877045 | intron variant | G/A | snv | 0.53 | 14 | ||
rs4774 | 0.807 | 0.240 | 16 | 10906991 | missense variant | G/C | snv | 0.30 | 0.28 | 7 | |
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs9634314 | 12 | 109968581 | intron variant | G/A | snv | 0.20 | 1 | ||||
rs10816914 | 9 | 109998608 | intron variant | G/A | snv | 0.40 | 1 | ||||
rs675605 | 13 | 110221209 | intron variant | G/A;C | snv | 1 | |||||
rs2855469 | 10 | 110281821 | intron variant | T/C | snv | 0.43 | 1 | ||||
rs1285539239 | 13 | 110462280 | missense variant | G/A | snv | 4.0E-06 | 1 |