Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17762454 | 0.925 | 0.120 | 6 | 7212967 | non coding transcript exon variant | C/T | snv | 0.25 | 4 | ||
rs11755724 | 0.807 | 0.320 | 6 | 7118757 | intron variant | A/G;T | snv | 3 | |||
rs1285874 | 0.925 | 0.120 | 6 | 7115300 | intron variant | T/A | snv | 0.66 | 2 | ||
rs1285875 | 0.925 | 0.120 | 6 | 7115694 | intron variant | G/A;C | snv | 0.63 | 2 | ||
rs1285879 | 0.925 | 0.120 | 6 | 7137130 | intron variant | T/C | snv | 0.67 | 2 | ||
rs1334577 | 0.925 | 0.120 | 6 | 7211518 | intron variant | G/A | snv | 0.23 | 2 | ||
rs2842895 | 0.925 | 0.120 | 6 | 7106083 | upstream gene variant | G/C | snv | 0.40 | 2 | ||
rs4585612 | 0.925 | 0.120 | 6 | 7152919 | intron variant | C/T | snv | 0.41 | 2 | ||
rs622404 | 0.925 | 0.120 | 6 | 7130363 | intron variant | A/G | snv | 0.68 | 2 | ||
rs630258 | 0.925 | 0.120 | 6 | 7134168 | intron variant | T/C | snv | 0.67 | 2 | ||
rs665723 | 0.925 | 0.120 | 6 | 7138831 | intron variant | C/T | snv | 0.67 | 2 | ||
rs687467 | 0.925 | 0.120 | 6 | 7127843 | intron variant | A/G;T | snv | 2 | |||
rs6933716 | 0.925 | 0.120 | 6 | 7125476 | intron variant | T/C | snv | 0.53 | 2 |