Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
rs11538209 | 1.000 | 0.120 | 4 | 73404356 | missense variant | T/C | snv | 2 | |||
rs58624704 | 0.925 | 0.200 | 4 | 73410325 | missense variant | G/A | snv | 8.0E-06 | 3.5E-05 | 2 | |
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 43 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs136161 | 0.925 | 0.160 | 22 | 36261386 | intron variant | G/C | snv | 0.51 | 3 | ||
rs3807337 | 1.000 | 0.120 | 7 | 134779071 | intron variant | A/G;T | snv | 1 | |||
rs3917887 | 0.776 | 0.240 | 17 | 34255979 | non coding transcript exon variant | AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC | delins | 0.33 | 8 | ||
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 12 | |||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 18 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 12 | ||
rs4783961 | 0.851 | 0.320 | 16 | 56960982 | upstream gene variant | G/A | snv | 0.48 | 0.47 | 7 | |
rs39075 | 1.000 | 0.120 | 7 | 29237076 | intron variant | G/A | snv | 0.41 | 1 | ||
rs805304 | 0.851 | 0.240 | 6 | 31730311 | 5 prime UTR variant | T/G | snv | 0.48 | 5 | ||
rs2346061 | 1.000 | 0.120 | 18 | 74533297 | upstream gene variant | C/A | snv | 0.71 | 1 | ||
rs7577 | 1.000 | 0.120 | 18 | 74521112 | 3 prime UTR variant | T/A;C;G | snv | 0.21 | 1 | ||
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs3742264 | 0.742 | 0.400 | 13 | 46073959 | missense variant | C/T | snv | 0.31 | 0.35 | 17 | |
rs1926447 | 0.807 | 0.440 | 13 | 46055809 | missense variant | A/G | snv | 0.74 | 0.77 | 11 | |
rs143101792 | 0.851 | 0.320 | 1 | 159714026 | stop gained | G/C | snv | 8.8E-05 | 1.3E-04 | 5 | |
rs762285755 | 0.925 | 0.160 | 10 | 17114074 | missense variant | T/C | snv | 7.6E-05 | 2.8E-05 | 2 | |
rs1252906 | 1.000 | 0.120 | 14 | 59192073 | intron variant | A/C;G | snv | 1 | |||
rs994411260 | 0.925 | 0.160 | 19 | 10194877 | missense variant | G/C | snv | 2 |