Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs866291718 | 1.000 | 0.040 | 4 | 39470042 | missense variant | A/G | snv | 3 | |||
rs751866383 | 1.000 | 0.040 | 4 | 39470047 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
rs1064797245 | 0.776 | 0.280 | 19 | 41970540 | missense variant | G/A | snv | 12 | |||
rs756632799 | 0.882 | 0.080 | 20 | 45416579 | stop gained | G/T | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs527236031 | 0.882 | 0.080 | 20 | 45424323 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 5 | |
rs752874517 | 1.000 | 0.080 | 20 | 45425779 | missense variant | C/A;T | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs786203999 | 1.000 | 16 | 46906858 | missense variant | C/G | snv | 2 | ||||
rs74315403 | 0.790 | 0.200 | 20 | 4699752 | missense variant | G/A | snv | 10 | |||
rs74315413 | 0.807 | 0.160 | 20 | 4699780 | missense variant | A/G | snv | 8 | |||
rs2239186 | 0.882 | 0.120 | 12 | 47875627 | intron variant | A/C;G | snv | 0.17 | 5 | ||
rs4516035 | 0.776 | 0.360 | 12 | 47906043 | non coding transcript exon variant | T/C | snv | 0.31 | 10 | ||
rs2229291 | 0.827 | 0.200 | 1 | 53210729 | missense variant | T/G | snv | 2.3E-02 | 1.5E-02 | 8 | |
rs1799821 | 0.827 | 0.200 | 1 | 53210776 | missense variant | G/A | snv | 0.49 | 0.46 | 8 | |
rs368311455 | 0.882 | 0.200 | 1 | 53211185 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 4 | |
rs751557097 | 1 | 53213431 | missense variant | G/C | snv | 2.8E-05 | 1 | ||||
rs397514611 | 1.000 | 6 | 5545261 | missense variant | T/C | snv | 1.2E-05 | 2 | |||
rs397514612 | 1.000 | 6 | 5613275 | missense variant | A/T | snv | 1.6E-05 | 7.0E-06 | 2 | ||
rs886041715 | 0.827 | 0.040 | 16 | 56192353 | missense variant | G/A;C;T | snv | 7 | |||
rs587777606 | 0.851 | 0.160 | 11 | 62691300 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs796052650 | 0.925 | 0.040 | 20 | 63413574 | missense variant | G/A;C | snv | 4 | |||
rs118192211 | 0.790 | 0.080 | 20 | 63439644 | missense variant | G/A;C | snv | 9 | |||
rs118192205 | 1.000 | 20 | 63442495 | missense variant | G/A | snv | 2 | ||||
rs1057516085 | 0.827 | 0.080 | 20 | 63444747 | missense variant | C/T | snv | 8 | |||
rs796052621 | 0.827 | 0.080 | 20 | 63444756 | missense variant | C/T | snv | 6 | |||
rs756762431 | 1.000 | 0.120 | 19 | 6495654 | missense variant | C/G;T | snv | 8.0E-06 | 2 |