Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11575886 | 1.000 | 0.080 | 20 | 56248494 | upstream gene variant | A/G | snv | 8.0E-02 | 1 | ||
rs1194182 | 1.000 | 0.080 | 7 | 80602188 | 5 prime UTR variant | G/C | snv | 0.53 | 2 | ||
rs121917864 | 0.645 | 0.520 | 4 | 153704936 | missense variant | C/T | snv | 8.8E-05 | 9.8E-05 | 31 | |
rs12212067 | 0.716 | 0.320 | 6 | 108659993 | intron variant | T/G | snv | 0.14 | 20 | ||
rs12477677 | 1.000 | 0.080 | 2 | 207666398 | intron variant | T/C | snv | 0.22 | 2 | ||
rs12596308 | 0.925 | 0.120 | 16 | 29679875 | intron variant | C/A;T | snv | 2 | |||
rs12998782 | 0.882 | 0.160 | 2 | 118967804 | intron variant | C/T | snv | 0.19 | 3 | ||
rs1327474 | 0.925 | 0.080 | 6 | 137219938 | upstream gene variant | C/T | snv | 0.67 | 2 | ||
rs1327475 | 0.925 | 0.080 | 6 | 137215318 | missense variant | G/A | snv | 0.13 | 0.12 | 2 | |
rs1371329921 | 0.925 | 0.080 | 9 | 117712993 | stop gained | C/T | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs1371562 | 1.000 | 0.080 | 2 | 118975372 | intron variant | G/T | snv | 0.33 | 1 | ||
rs1372834938 | 0.763 | 0.280 | 2 | 8812465 | missense variant | G/C | snv | 4.2E-06 | 12 | ||
rs138968705 | 0.925 | 0.080 | 4 | 38828278 | missense variant | G/A | snv | 1.2E-04 | 2.3E-04 | 2 | |
rs141555015 | 1.000 | 0.080 | 6 | 32839023 | upstream gene variant | GCTTTGTAATTGGAGAAT/- | delins | 1.4E-05 | 1 | ||
rs1518111 | 0.790 | 0.360 | 1 | 206771300 | intron variant | T/C | snv | 0.71 | 9 | ||
rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
rs15493 | 1.000 | 0.080 | 14 | 67651415 | missense variant | C/G;T | snv | 9.2E-02 | 8.8E-02 | 1 | |
rs1554286 | 0.790 | 0.320 | 1 | 206770888 | 5 prime UTR variant | A/G;T | snv | 0.72 | 7 | ||
rs1568952 | 1.000 | 0.080 | 8 | 58799804 | intergenic variant | T/C | snv | 0.75 | 1 | ||
rs16826860 | 1.000 | 0.080 | 2 | 230182908 | intron variant | G/A | snv | 7.2E-02 | 1 | ||
rs17009726 | 1.000 | 0.080 | 2 | 118967884 | intron variant | A/G | snv | 1.0E-02 | 1 | ||
rs1718119 | 0.689 | 0.520 | 12 | 121177300 | missense variant | G/A;T | snv | 0.35; 4.0E-06 | 21 | ||
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 | ||
rs17795618 | 1.000 | 0.080 | 2 | 118973892 | intron variant | T/A | snv | 0.12 | 1 | ||
rs17842268 | 0.925 | 0.120 | 16 | 29672859 | intron variant | T/C | snv | 0.36 | 2 |