Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2517713 | 1.000 | 0.120 | 6 | 29950322 | downstream gene variant | G/A;T | snv | 1 | |||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 1 | |||
rs3094146 | 1.000 | 0.080 | 6 | 30003183 | non coding transcript exon variant | G/C | snv | 6.1E-02 | 1 | ||
rs114577328 | 1.000 | 0.080 | 6 | 29959505 | downstream gene variant | G/C | snv | 1.3E-02 | 1 | ||
rs2523933 | 6 | 29964515 | intergenic variant | G/C;T | snv | 1 | |||||
rs2394250 | 1.000 | 0.040 | 6 | 29975879 | intron variant | G/T | snv | 0.40 | 1 | ||
rs9259819 | 6 | 29925798 | upstream gene variant | G/T | snv | 0.49 | 1 | ||||
rs1061539 | 1.000 | 0.040 | 6 | 29969778 | downstream gene variant | T/A;C | snv | 1 | |||
rs9260489 | 1.000 | 0.080 | 6 | 29952555 | upstream gene variant | T/A;G | snv | 2 | |||
rs115625073 | 1.000 | 0.040 | 6 | 29924456 | upstream gene variant | T/C | snv | 2 | |||
rs144304366 | 1.000 | 0.040 | 6 | 29936216 | downstream gene variant | T/C | snv | 2 | |||
rs9260313 | 6 | 29949108 | downstream gene variant | T/C | snv | 0.42 | 2 | ||||
rs6914699 | 6 | 29966245 | downstream gene variant | T/C | snv | 0.41 | 1 | ||||
rs150881176 | 1.000 | 0.120 | 6 | 29979963 | downstream gene variant | T/C | snv | 1 | |||
rs115729734 | 1.000 | 0.080 | 6 | 29931238 | upstream gene variant | T/C;G | snv | 1 | |||
rs9260620 | 6 | 29955314 | upstream gene variant | T/G | snv | 0.24 | 7 | ||||
rs7758512 | 1.000 | 6 | 30002812 | intron variant | T/G | snv | 0.17 | 4 | |||
rs111312615 | 1.000 | 0.040 | 6 | 29955302 | upstream gene variant | T/G | snv | 2 | |||
rs60131261 | 1.000 | 0.040 | 6 | 29969559 | downstream gene variant | TTTA/- | delins | 0.26 | 1 |