Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1075309 | 1.000 | 0.040 | 2 | 5113465 | intergenic variant | C/T | snv | 0.20 | 1 | ||
rs11031728 | 1.000 | 0.040 | 11 | 32342070 | intron variant | C/G | snv | 0.18 | 1 | ||
rs12437118 | 1.000 | 0.040 | 14 | 76517387 | intron variant | G/A;C | snv | 1 | |||
rs12456774 | 1.000 | 0.040 | 18 | 22592612 | intergenic variant | G/A | snv | 0.17 | 1 | ||
rs17175227 | 1.000 | 0.040 | 14 | 70035333 | downstream gene variant | G/A;C | snv | 2.1E-02 | 1 | ||
rs2057178 | 1.000 | 0.040 | 11 | 32342641 | intron variant | G/A | snv | 0.18 | 1 | ||
rs2202157 | 1.000 | 0.040 | 3 | 26501929 | intergenic variant | C/T | snv | 0.12 | 1 | ||
rs39509 | 1.000 | 0.040 | 8 | 89791937 | downstream gene variant | G/A | snv | 0.65 | 1 | ||
rs4859843 | 1.000 | 0.040 | 4 | 77439033 | intron variant | T/C;G | snv | 1 | |||
rs4859846 | 1.000 | 0.040 | 4 | 77439174 | intron variant | G/A | snv | 0.19 | 1 | ||
rs6676375 | 1.000 | 0.040 | 1 | 242711583 | intergenic variant | T/C | snv | 0.15 | 1 | ||
rs8087945 | 1.000 | 0.040 | 18 | 22596123 | intergenic variant | A/G | snv | 0.61 | 1 | ||
rs932347 | 1.000 | 0.040 | 1 | 209882285 | intergenic variant | C/T | snv | 0.15 | 1 | ||
rs958617 | 1.000 | 0.040 | 4 | 77684215 | intergenic variant | A/G | snv | 0.56 | 1 | ||
rs2542670 | 1.000 | 0.040 | 17 | 37294135 | intron variant | A/G;T | snv | 1 | |||
rs2115819 | 1.000 | 0.040 | 10 | 45405641 | intron variant | A/G | snv | 0.42 | 1 | ||
rs7111432 | 1.000 | 0.040 | 11 | 429659 | splice region variant | C/G;T | snv | 4.0E-06; 0.56 | 1 | ||
rs1017281 | 1.000 | 0.040 | 8 | 130234967 | intron variant | G/A | snv | 0.37 | 1 | ||
rs10956514 | 1.000 | 0.040 | 8 | 130240512 | intron variant | A/G | snv | 0.37 | 1 | ||
rs11774633 | 1.000 | 0.040 | 8 | 130177997 | intron variant | C/T | snv | 0.61 | 1 | ||
rs4236749 | 1.000 | 0.040 | 8 | 130052907 | 3 prime UTR variant | C/T | snv | 0.16 | 1 | ||
rs4733781 | 1.000 | 0.040 | 8 | 130284521 | intron variant | A/C | snv | 0.29 | 1 | ||
rs1925714 | 1.000 | 0.040 | 1 | 228515588 | upstream gene variant | A/G | snv | 0.81 | 1 | ||
rs451390 | 1.000 | 0.040 | 21 | 41923401 | intron variant | G/C | snv | 7.5E-02 | 1 | ||
rs411089 | 1.000 | 0.040 | 1 | 158255035 | intron variant | C/T | snv | 0.39 | 0.43 | 1 |