Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 8 | ||
rs13394720 | 1.000 | 2 | 233593475 | intergenic variant | T/C | snv | 7.0E-02 | 6 | |||
rs887829 | 0.763 | 0.280 | 2 | 233759924 | intron variant | C/T | snv | 0.36 | 6 | ||
rs4149056 | 0.633 | 0.480 | 12 | 21178615 | missense variant | T/C | snv | 0.13 | 0.12 | 5 | |
rs11563251 | 2 | 233770738 | 3 prime UTR variant | C/T | snv | 0.19 | 5 | ||||
rs1550532 | 2 | 233356202 | intron variant | C/G | snv | 0.75 | 4 | ||||
rs4149081 | 1.000 | 0.040 | 12 | 21225087 | intron variant | G/A | snv | 0.18 | 4 | ||
rs11891311 | 2 | 233730664 | intron variant | G/A | snv | 0.42 | 4 | ||||
rs17864661 | 2 | 233587096 | downstream gene variant | C/T | snv | 0.14 | 3 | ||||
rs2602362 | 2 | 233607902 | downstream gene variant | A/C | snv | 0.22 | 3 | ||||
rs2602363 | 2 | 233611879 | intergenic variant | T/C | snv | 0.22 | 3 | ||||
rs2602364 | 2 | 233615583 | upstream gene variant | G/A | snv | 0.22 | 3 | ||||
rs2741019 | 2 | 233602042 | upstream gene variant | C/A;G | snv | 3 | |||||
rs2741021 | 2 | 233603237 | upstream gene variant | C/T | snv | 0.22 | 3 | ||||
rs2741027 | 1.000 | 0.040 | 2 | 233609365 | downstream gene variant | G/A | snv | 0.22 | 3 | ||
rs2741028 | 2 | 233610268 | intergenic variant | G/A;T | snv | 3 | |||||
rs11694406 | 2 | 233423164 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs6741669 | 2 | 233744546 | intron variant | A/G | snv | 0.55 | 3 | ||||
rs11045879 | 1.000 | 0.120 | 12 | 21229685 | intron variant | T/C | snv | 0.18 | 3 | ||
rs2417940 | 12 | 20864941 | intron variant | T/A;C | snv | 3 | |||||
rs4148324 | 2 | 233764076 | intron variant | T/A;G | snv | 0.36 | 3 | ||||
rs6715325 | 2 | 233726595 | intron variant | T/C | snv | 0.46 | 3 | ||||
rs10175809 | 2 | 233688219 | intron variant | T/A | snv | 0.39 | 3 | ||||
rs11892031 | 0.882 | 0.120 | 2 | 233656637 | intron variant | A/C;T | snv | 3 | |||
rs2741034 | 2 | 233640168 | intron variant | A/G | snv | 0.22 | 3 |