Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs115960997 | 1.000 | 0.040 | 6 | 29934332 | downstream gene variant | G/A;T | snv | 2 | |||
rs111312615 | 1.000 | 0.040 | 6 | 29955302 | upstream gene variant | T/G | snv | 2 | |||
rs144304366 | 1.000 | 0.040 | 6 | 29936216 | downstream gene variant | T/C | snv | 2 | |||
rs114950038 | 1.000 | 0.040 | 6 | 29983056 | downstream gene variant | G/A;C | snv | 2 | |||
rs9260489 | 1.000 | 0.080 | 6 | 29952555 | upstream gene variant | T/A;G | snv | 2 | |||
rs115928623 | 1.000 | 0.080 | 6 | 29971371 | intron variant | A/T | snv | 1 | |||
rs115559990 | 6 | 29926633 | non coding transcript exon variant | C/G;T | snv | 1 | |||||
rs2523946 | 0.925 | 0.200 | 6 | 29974166 | upstream gene variant | C/A;G;T | snv | 1 | |||
rs2523933 | 6 | 29964515 | intergenic variant | G/C;T | snv | 1 | |||||
rs150881176 | 1.000 | 0.120 | 6 | 29979963 | downstream gene variant | T/C | snv | 1 | |||
rs2860580 | 1.000 | 0.120 | 6 | 29938914 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs2517713 | 1.000 | 0.120 | 6 | 29950322 | downstream gene variant | G/A;T | snv | 1 | |||
rs1061539 | 1.000 | 0.040 | 6 | 29969778 | downstream gene variant | T/A;C | snv | 1 | |||
rs3823355 | 1.000 | 0.040 | 6 | 29974306 | upstream gene variant | C/A;T | snv | 1 | |||
rs41546314 | 1.000 | 0.040 | 6 | 29942601 | synonymous variant | C/T | snv | 0.26 | 1 | ||
rs147097402 | 1.000 | 0.080 | 6 | 29930083 | upstream gene variant | C/A;G;T | snv | 1 | |||
rs115729734 | 1.000 | 0.080 | 6 | 29931238 | upstream gene variant | T/C;G | snv | 1 | |||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 1 | |||
rs28749114 | 6 | 29937675 | upstream gene variant | A/G;T | snv | 1 |