Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12720459 | 0.807 | 0.160 | 11 | 2583535 | missense variant | C/A;G;T | snv | 7 | |||
rs755221106 | 0.851 | 0.040 | 17 | 50617560 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
rs267607277 | 0.807 | 0.120 | 14 | 90404386 | missense variant | A/G | snv | 6 | |||
rs398124647 | 0.807 | 0.120 | 2 | 47161851 | missense variant | T/A;C | snv | 6 | |||
rs786205745 | 0.807 | 0.320 | 12 | 2504538 | missense variant | G/A;C | snv | 6 | |||
rs587782933 | 0.827 | 0.200 | 12 | 2504526 | missense variant | G/A | snv | 5 | |||
rs587777598 | 0.851 | 0.200 | 6 | 79921662 | missense variant | C/G;T | snv | 4 | |||
rs11567847 | 0.925 | 0.120 | 11 | 12937202 | missense variant | T/C | snv | 3 | |||
rs1208917022 | 1.000 | 0.040 | 12 | 6936663 | missense variant | A/G | snv | 3 | |||
rs1458500258 | 0.925 | 0.080 | 1 | 237388098 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
rs192749597 | 0.882 | 0.080 | 12 | 2679712 | missense variant | C/T | snv | 9.2E-04 | 3.5E-03 | 3 | |
rs786205753 | 0.925 | 0.080 | 12 | 2593255 | missense variant | G/A | snv | 3 | |||
rs80315385 | 0.882 | 0.200 | 12 | 2504932 | missense variant | G/A | snv | 3 | |||
rs104894393 | 0.925 | 0.120 | 13 | 101726785 | missense variant | A/G | snv | 2 | |||
rs1805323 | 0.925 | 0.160 | 7 | 5987311 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-02 | 2 | ||
rs3734960 | 0.925 | 0.240 | 7 | 154892443 | missense variant | T/C | snv | 0.33 | 0.36 | 2 | |
rs606231451 | 0.925 | 0.120 | 1 | 1535372 | missense variant | G/A | snv | 2 | |||
rs138694505 | 1.000 | 0.040 | 7 | 84007493 | missense variant | T/C | snv | 3.4E-03 | 6.6E-03 | 1 | |
rs149767043 | 1.000 | 0.040 | 20 | 3343726 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs4149000 | 0.882 | 0.080 | 12 | 21295063 | non coding transcript exon variant | C/T | snv | 0.11 | 5 | ||
rs7208480 | 1.000 | 0.040 | 17 | 15770470 | non coding transcript exon variant | C/T | snv | 0.28 | 1 | ||
rs3512 | 0.925 | 0.160 | 15 | 30942802 | 3 prime UTR variant | G/C | snv | 0.27 | 4 | ||
rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
rs16847548 | 0.807 | 0.120 | 1 | 162065484 | upstream gene variant | T/C | snv | 0.22 | 8 |