Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
rs2975009 | 6 | 29930339 | upstream gene variant | C/T | snv | 0.50 | 1 | ||||
rs1061539 | 1.000 | 0.040 | 6 | 29969778 | downstream gene variant | T/A;C | snv | 1 | |||
rs60131261 | 1.000 | 0.040 | 6 | 29969559 | downstream gene variant | TTTA/- | delins | 0.26 | 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 | |||
rs17882753 | 6 | 29944817 | non coding transcript exon variant | C/T | snv | 1.4E-02 | 1 | ||||
rs115729734 | 1.000 | 0.080 | 6 | 29931238 | upstream gene variant | T/C;G | snv | 1 | |||
rs16896742 | 6 | 29954963 | upstream gene variant | A/G | snv | 0.35 | 1 | ||||
rs28749114 | 6 | 29937675 | upstream gene variant | A/G;T | snv | 1 | |||||
rs114577328 | 1.000 | 0.080 | 6 | 29959505 | downstream gene variant | G/C | snv | 1.3E-02 | 1 | ||
rs9259819 | 6 | 29925798 | upstream gene variant | G/T | snv | 0.49 | 1 | ||||
rs2394250 | 1.000 | 0.040 | 6 | 29975879 | intron variant | G/T | snv | 0.40 | 1 | ||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 1 | |||
rs2517873 | 1.000 | 0.080 | 6 | 29908215 | intron variant | G/A | snv | 0.15 | 1 | ||
rs115928623 | 1.000 | 0.080 | 6 | 29971371 | intron variant | A/T | snv | 1 | |||
rs3094146 | 1.000 | 0.080 | 6 | 30003183 | non coding transcript exon variant | G/C | snv | 6.1E-02 | 1 |