Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs779027563 | 0.677 | 0.360 | 17 | 42687838 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 58 | |
rs780533096 | 0.701 | 0.600 | 13 | 23886338 | missense variant | C/G;T | snv | 4.8E-06; 9.6E-06 | 44 | ||
rs1555968941 | 0.752 | 0.280 | 12 | 2653847 | missense variant | G/A;C | snv | 31 | |||
rs34757931 | 0.742 | 0.360 | 11 | 119081189 | missense variant | T/G | snv | 1.2E-04 | 5.6E-05 | 26 | |
rs886041091 | 0.807 | 0.120 | 9 | 84751990 | missense variant | A/G | snv | 18 | |||
rs387906799 | 0.742 | 0.200 | 2 | 240788118 | missense variant | G/A | snv | 17 | |||
rs1555817157 | 0.742 | 0.280 | 20 | 25339320 | frameshift variant | TCTTCCTCAGGCG/- | del | 16 | |||
rs753611141 | 0.827 | 0.280 | 9 | 136418847 | missense variant | G/A;T | snv | 2.4E-05; 4.0E-06 | 14 | ||
rs672601370 | 0.790 | 0.160 | 2 | 240775863 | missense variant | G/A | snv | 13 | |||
rs768643552 | 0.851 | 0.240 | 9 | 136418630 | missense variant | G/A;C | snv | 4.0E-06 | 13 | ||
rs672601369 | 0.790 | 0.120 | 2 | 240783780 | missense variant | C/T | snv | 10 | |||
rs374997012 | 0.851 | 0.280 | 10 | 100989114 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 9 | |
rs886037832 | 0.851 | 0.280 | 10 | 100988541 | frameshift variant | T/- | delins | 9 | |||
rs730882246 | 0.807 | 0.200 | 14 | 74494329 | missense variant | G/A | snv | 8 | |||
rs756421370 | 0.807 | 0.120 | 1 | 29200513 | splice donor variant | -/A | delins | 1.4E-04 | 6.3E-05 | 8 | |
rs672601367 | 0.851 | 0.080 | 2 | 240785066 | missense variant | T/G | snv | 7 | |||
rs672601363 | 0.851 | 0.080 | 2 | 240788109 | missense variant | C/T | snv | 6 | |||
rs672601366 | 0.851 | 0.120 | 2 | 240786339 | missense variant | C/G | snv | 6 | |||
rs139194636 | 0.882 | 0.240 | 1 | 119033203 | missense variant | T/C | snv | 6.4E-05 | 2.3E-04 | 6 | |
rs757600616 | 0.882 | 0.240 | 1 | 119033279 | stop gained | G/A | snv | 1.2E-05 | 6 | ||
rs1057517686 | 0.827 | 0.120 | 1 | 1529299 | missense variant | C/T | snv | 5 | |||
rs1555303073 | 0.851 | 0.120 | 13 | 110176912 | missense variant | C/T | snv | 5 | |||
rs2157719 | 0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 | 4 |