Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2060793 | 0.776 | 0.240 | 11 | 14893764 | upstream gene variant | A/G | snv | 0.63 | 11 | ||
rs966423 | 0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv | 11 | |||
rs1867277 | 0.776 | 0.160 | 9 | 97853632 | 5 prime UTR variant | A/G | snv | 0.63 | 10 | ||
rs2439302 | 0.776 | 0.200 | 8 | 32574851 | intron variant | G/C | snv | 0.54 | 9 | ||
rs17849071 | 0.776 | 0.160 | 3 | 179218439 | intron variant | T/G | snv | 7.9E-02 | 8 | ||
rs3783521 | 0.807 | 0.200 | 2 | 112786000 | upstream gene variant | G/A | snv | 0.26 | 8 | ||
rs1064795638 | 0.851 | 0.080 | 3 | 52403251 | stop gained | G/A | snv | 7 | |||
rs6013897 | 0.790 | 0.200 | 20 | 54125940 | regulatory region variant | T/A | snv | 0.23 | 7 | ||
rs3917225 | 0.807 | 0.160 | 2 | 102152842 | intron variant | A/G | snv | 0.36 | 6 | ||
rs768827923 | 0.851 | 0.080 | 1 | 9721816 | missense variant | T/G | snv | 6 | |||
rs7850258 | 0.827 | 0.200 | 9 | 97786731 | intron variant | A/G | snv | 0.72 | 6 | ||
rs360718 | 0.827 | 0.120 | 11 | 112164016 | 5 prime UTR variant | A/C | snv | 0.26 | 5 | ||
rs786203472 | 0.827 | 0.120 | 22 | 28719414 | start lost | T/C | snv | 5 | |||
rs863224748 | 0.827 | 0.120 | 22 | 28734721 | start lost | T/C | snv | 5 | |||
rs1248131654 | 0.851 | 0.080 | 2 | 160367217 | missense variant | G/A | snv | 1.4E-05 | 4 | ||
rs13143866 | 0.851 | 0.200 | 4 | 122619603 | intron variant | G/A | snv | 0.24 | 4 | ||
rs1443434 | 0.851 | 0.080 | 9 | 97855197 | 3 prime UTR variant | G/T | snv | 0.63 | 4 | ||
rs1946519 | 0.851 | 0.120 | 11 | 112164784 | intron variant | A/C | snv | 0.60 | 4 | ||
rs360717 | 0.851 | 0.080 | 11 | 112164002 | 5 prime UTR variant | G/A | snv | 0.25 | 4 | ||
rs7028661 | 0.882 | 0.080 | 9 | 97776188 | intron variant | A/G | snv | 0.72 | 4 | ||
rs71369530 | 0.851 | 0.080 | 9 | 97854419 | inframe insertion | GCCGCCGCCGCCGCCGCCGCCGCC/-;GCC;GCCGCC;GCCGCCGCC;GCCGCCGCCGCC;GCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC | delins | 0.68 | 4 | ||
rs907580 | 0.851 | 0.080 | 9 | 97860315 | downstream gene variant | T/A;C;G | snv | 4 | |||
rs1031583860 | 0.882 | 0.080 | 11 | 58709815 | missense variant | T/C | snv | 3 | |||
rs10951937 | 0.882 | 0.080 | 7 | 47992027 | intron variant | A/C | snv | 0.43 | 3 | ||
rs12769288 | 0.882 | 0.080 | 10 | 129488086 | intron variant | C/T | snv | 0.10 | 3 |