Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10230087 | 1.000 | 0.040 | 7 | 114614352 | intron variant | G/A | snv | 0.73 | 2 | ||
rs1023159 | 1.000 | 0.040 | 21 | 45546266 | intron variant | G/A | snv | 0.34 | 1 | ||
rs1026306398 | 1.000 | 0.040 | 7 | 155458802 | missense variant | C/A;G;T | snv | 3.0E-04; 7.6E-05 | 1 | ||
rs1033810883 | 1.000 | 0.040 | 12 | 48979625 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
rs10418707 | 1.000 | 0.040 | 19 | 10145541 | intron variant | G/A;T | snv | 0.11 | 1 | ||
rs10423341 | 1.000 | 0.040 | 19 | 10156590 | intron variant | C/A | snv | 0.13 | 1 | ||
rs1042778 | 0.925 | 0.040 | 3 | 8752859 | 3 prime UTR variant | G/A;C;T | snv | 3 | |||
rs1049346 | 0.882 | 0.080 | 6 | 38703061 | 5 prime UTR variant | G/A | snv | 0.50 | 0.54 | 3 | |
rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 2 | |||
rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 3 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs1051312 | 0.827 | 0.120 | 20 | 10306440 | 3 prime UTR variant | T/C | snv | 0.20 | 5 | ||
rs1060826 | 0.851 | 0.160 | 17 | 27762841 | synonymous variant | T/C | snv | 0.66 | 0.67 | 4 | |
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 34 | ||
rs1085308043 | 0.763 | 0.200 | 10 | 87925511 | splice acceptor variant | A/G;T | snv | 12 | |||
rs10877969 | 0.882 | 0.120 | 12 | 63153459 | intron variant | T/C | snv | 0.26 | 6 | ||
rs10951154 | 0.925 | 0.040 | 7 | 27095695 | missense variant | C/A;G;T | snv | 0.76 | 2 | ||
rs11155819 | 1.000 | 0.040 | 6 | 151878224 | intron variant | T/C | snv | 0.25 | 1 | ||
rs11236697 | 1.000 | 0.040 | 11 | 70576391 | intron variant | T/C | snv | 4.4E-02 | 1 | ||
rs112795301 | 0.776 | 0.160 | 3 | 70972634 | stop gained | G/A | snv | 13 | |||
rs1131692040 | 0.882 | 0.160 | X | 154399844 | missense variant | A/G | snv | 4 | |||
rs1152582 | 1.000 | 0.040 | 14 | 64225912 | 3 prime UTR variant | G/A;C | snv | 1 | |||
rs1163276899 | 1.000 | 0.040 | 3 | 53673125 | missense variant | G/A | snv | 2 | |||
rs11639084 | 0.851 | 0.200 | 15 | 60774317 | intron variant | C/T | snv | 0.20 | 4 | ||
rs11787216 | 1.000 | 0.040 | 8 | 141605122 | intron variant | C/T | snv | 0.26 | 2 |