Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3781719 | 1.000 | 0.040 | 11 | 14972978 | intron variant | A/G | snv | 0.35 | 2 | ||
rs614230 | 1.000 | 0.040 | 16 | 57385374 | downstream gene variant | C/T | snv | 0.61 | 2 | ||
rs200207721 | 6 | 154039743 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 2 | |||
rs77114424 | 6 | 154039497 | missense variant | G/A | snv | 2 | |||||
rs41292285 | 1.000 | 0.040 | 16 | 1208033 | missense variant | G/T | snv | 7.3E-03 | 7.1E-03 | 3 | |
rs540638287 | 1.000 | 0.040 | 16 | 1204313 | missense variant | C/T | snv | 4.3E-05 | 1.4E-05 | 3 | |
rs10877969 | 0.882 | 0.120 | 12 | 63153459 | intron variant | T/C | snv | 0.26 | 6 | ||
rs769540300 | 0.851 | 0.200 | 6 | 154091047 | missense variant | G/A | snv | 1.2E-05 | 8 | ||
rs1800866 | 0.851 | 0.080 | 9 | 34637693 | missense variant | T/G | snv | 0.20 | 0.18 | 8 | |
rs28936375 | 0.752 | 0.320 | 1 | 53197092 | missense variant | C/A | snv | 1.7E-04 | 2.2E-04 | 15 | |
rs3800373 | 0.752 | 0.200 | 6 | 35574699 | 3 prime UTR variant | C/A | snv | 0.68 | 22 | ||
rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
rs80338903 | 0.701 | 0.360 | 1 | 216247095 | frameshift variant | C/- | del | 7.6E-04 | 5.4E-04 | 25 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 |