Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3745601 | 0.882 | 0.120 | 19 | 10113872 | missense variant | G/A | snv | 0.16 | 0.13 | 3 | |
rs1050286 | 0.882 | 0.160 | 12 | 10158964 | 3 prime UTR variant | T/C | snv | 0.40 | 3 | ||
rs3736235 | 0.925 | 0.080 | 12 | 10160476 | non coding transcript exon variant | T/C | snv | 0.43 | 0.40 | 2 | |
rs11053646 | 0.724 | 0.280 | 12 | 10160849 | missense variant | C/G | snv | 0.11 | 0.13 | 18 | |
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs1122608 | 0.763 | 0.120 | 19 | 11052925 | intron variant | G/T | snv | 0.18 | 16 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs200478651 | 1.000 | 0.080 | 13 | 113118414 | splice region variant | C/A;T | snv | 8.4E-06; 2.1E-05 | 1 | ||
rs1183027238 | 1.000 | 0.080 | 13 | 113118480 | synonymous variant | C/T | snv | 1 | |||
rs201058276 | 0.776 | 0.240 | 13 | 113118731 | missense variant | G/A;C | snv | 4.8E-05; 4.0E-06 | 11 | ||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 34 | |
rs12375498 | 1.000 | 0.080 | 9 | 116187719 | synonymous variant | C/T | snv | 0.19 | 0.17 | 1 | |
rs13290387 | 0.925 | 0.120 | 9 | 116227647 | intron variant | G/C | snv | 0.54 | 2 | ||
rs1191926239 | 0.807 | 0.200 | 9 | 117704539 | missense variant | C/G | snv | 4.0E-06 | 7 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs1255283120 | 0.807 | 0.160 | 1 | 11792345 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 7 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1217035505 | 1.000 | 0.080 | 12 | 121184674 | missense variant | G/A | snv | 1 | |||
rs775913429 | 1.000 | 0.080 | 12 | 132620455 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs2804924 | 1.000 | 0.080 | 6 | 13574110 | upstream gene variant | G/A;C;T | snv | 1 | |||
rs112443954 | 1.000 | 0.080 | 6 | 13574259 | upstream gene variant | G/C | snv | 0.27 | 1 | ||
rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
rs4636297 | 0.724 | 0.360 | 9 | 136670698 | intron variant | A/G | snv | 0.67 | 0.65 | 14 | |
rs1140713 | 1.000 | 0.080 | 9 | 136670833 | intron variant | C/T | snv | 0.13 | 1 |