Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2186607 | 0.776 | 0.080 | 11 | 101785666 | intron variant | T/A | snv | 0.51 | 10 | ||
rs188096 | 1.000 | 0.080 | 13 | 103052694 | missense variant | A/C | snv | 0.85 | 0.89 | 1 | |
rs41281678 | 1.000 | 0.080 | 13 | 103052700 | synonymous variant | G/A | snv | 1.9E-02 | 2.7E-02 | 1 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs1391441 | 0.763 | 0.240 | 4 | 105207603 | intron variant | G/A | snv | 0.70 | 11 | ||
rs1078643 | 0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv | 10 | |||
rs768623239 | 0.662 | 0.640 | 1 | 109689278 | missense variant | A/G | snv | 1.5E-05 | 26 | ||
rs1376251 | 0.882 | 0.160 | 12 | 10986253 | missense variant | C/T | snv | 0.40 | 0.28 | 3 | |
rs8000189 | 0.776 | 0.080 | 13 | 110423534 | intron variant | C/T | snv | 0.61 | 10 | ||
rs10980628 | 0.776 | 0.080 | 9 | 110909123 | intron variant | T/C | snv | 0.16 | 10 | ||
rs3087967 | 0.776 | 0.080 | 11 | 111286111 | 3 prime UTR variant | T/C | snv | 0.72 | 10 | ||
rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
rs201745983 | 0.752 | 0.200 | 12 | 111783219 | missense variant | G/A | snv | 6.8E-05 | 7.7E-05 | 14 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs12246635 | 0.776 | 0.080 | 10 | 112528860 | intron variant | T/C | snv | 0.13 | 10 | ||
rs755229494 | 0.776 | 0.080 | 5 | 112761654 | intron variant | A/G | snv | 9.6E-04 | 10 | ||
rs762117133 | 1.000 | 0.080 | 5 | 112801324 | missense variant | C/A;T | snv | 2.4E-05 | 3 | ||
rs770649674 | 0.807 | 0.120 | 5 | 112827177 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs1463038513 | 0.658 | 0.440 | 5 | 112839511 | frameshift variant | TAAA/- | delins | 36 | |||
rs1801155 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 42 | |
rs1801166 | 0.732 | 0.200 | 5 | 112839543 | missense variant | G/C | snv | 4.4E-03 | 5.6E-03 | 17 | |
rs11196170 | 0.776 | 0.080 | 10 | 112962862 | intron variant | G/A;C | snv | 10 | |||
rs13086367 | 0.776 | 0.080 | 3 | 113185041 | downstream gene variant | A/G | snv | 0.38 | 10 | ||
rs72942485 | 0.776 | 0.080 | 3 | 113280713 | intron variant | G/A | snv | 2.7E-02 | 4.5E-02 | 10 | |
rs1427760 | 0.776 | 0.080 | 12 | 114662909 | upstream gene variant | T/C | snv | 0.49 | 10 |