Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs6318 | 0.623 | 0.520 | X | 114731326 | missense variant | C/G;T | snv | 42 | |||
rs995922697 | 0.724 | 0.560 | 3 | 49357413 | missense variant | A/G | snv | 4.1E-06 | 15 | ||
rs3730358 | 0.724 | 0.360 | 14 | 104780070 | intron variant | G/A;C | snv | 0.16; 4.0E-03 | 14 | ||
rs10828317 | 0.776 | 0.280 | 10 | 22550699 | missense variant | T/C | snv | 9 | |||
rs781598341 | 0.827 | 0.240 | 6 | 159682510 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs1182593032 | 0.851 | 0.200 | 16 | 69718516 | missense variant | A/G | snv | 4 | |||
rs1231813088 | 0.851 | 0.160 | 10 | 92690015 | missense variant | C/T | snv | 4 | |||
rs1322425552 | 0.851 | 0.160 | 17 | 74923048 | missense variant | G/A | snv | 4 | |||
rs1457049406 | 0.851 | 0.200 | 22 | 19962555 | missense variant | C/T | snv | 4 | |||
rs6805251 | 0.925 | 0.120 | 3 | 119841759 | intron variant | T/A;C | snv | 4 | |||
rs1402139464 | 0.882 | 0.160 | 11 | 27701009 | 5 prime UTR variant | G/A;T | snv | 8.4E-06 | 3 | ||
rs1447119000 | 0.925 | 0.120 | 22 | 42130763 | missense variant | G/A | snv | 2 | |||
rs1890196 | 0.925 | 0.120 | 1 | 66337397 | intron variant | C/G;T | snv | 2 | |||
rs2445142 | 0.925 | 0.120 | 1 | 21899250 | intron variant | G/A;C | snv | 2 | |||
rs2701124 | 0.925 | 0.120 | 12 | 52054373 | synonymous variant | G/A;C | snv | 9.5E-02 | 2 | ||
rs6587002 | 0.925 | 0.120 | 8 | 21723708 | intron variant | T/C;G | snv | 2 | |||
rs767413934 | 0.925 | 0.120 | 11 | 113424539 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs905568 | 0.925 | 0.120 | 3 | 114232449 | non coding transcript exon variant | C/A;G;T | snv | 2 | |||
rs1258159645 | 0.630 | 0.600 | 16 | 69711128 | missense variant | G/A | snv | 7.0E-06 | 37 | ||
rs1322643228 | 0.807 | 0.280 | 12 | 104321110 | missense variant | C/T | snv | 7.1E-06 | 6 | ||
rs1330075052 | 0.882 | 0.160 | 12 | 104215828 | missense variant | T/C | snv | 1.4E-05 | 3 | ||
rs76980269 | 0.763 | 0.280 | 12 | 117330794 | synonymous variant | G/A | snv | 2.8E-05 | 4.2E-05 | 10 | |
rs201934979 | 0.882 | 0.160 | 15 | 74749838 | missense variant | C/T | snv | 8.8E-05; 8.0E-06 | 1.3E-04 | 3 |