Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 7 | ||
rs9368699 | 0.851 | 0.200 | 6 | 31834764 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 7 | ||
rs2260000 | 0.851 | 0.200 | 6 | 31625699 | intron variant | A/G | snv | 0.29 | 6 | ||
rs3093662 | 0.851 | 0.200 | 6 | 31576412 | intron variant | A/G | snv | 7.1E-02 | 6 | ||
rs6906846 | 0.851 | 0.280 | 6 | 31277959 | non coding transcript exon variant | A/G | snv | 0.67 | 6 | ||
rs12191877 | 0.851 | 0.120 | 6 | 31285148 | intron variant | C/T | snv | 0.12 | 5 | ||
rs4148325 | 0.851 | 0.080 | 2 | 233764663 | intron variant | C/T | snv | 0.36 | 3 | ||
rs2247056 | 0.882 | 0.160 | 6 | 31297713 | intron variant | T/C | snv | 0.80 | 8 | ||
rs2516509 | 0.882 | 0.160 | 6 | 31482217 | intron variant | T/C | snv | 0.19 | 7 | ||
rs2156875 | 0.882 | 0.200 | 6 | 31349570 | intron variant | C/T | snv | 0.50 | 6 | ||
rs2534657 | 0.882 | 0.200 | 6 | 31504682 | intron variant | C/T | snv | 0.15 | 6 | ||
rs259919 | 0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 | 6 | ||
rs2736172 | 0.882 | 0.160 | 6 | 31623121 | non coding transcript exon variant | C/T | snv | 0.41 | 0.29 | 6 | |
rs2844509 | 0.882 | 0.160 | 6 | 31543147 | intron variant | A/G | snv | 0.23 | 6 | ||
rs2856997 | 0.882 | 0.200 | 6 | 32813999 | non coding transcript exon variant | C/A | snv | 0.45 | 6 | ||
rs2894207 | 0.882 | 0.160 | 6 | 31295974 | intron variant | T/C | snv | 0.20 | 6 | ||
rs3130473 | 0.882 | 0.160 | 6 | 31231431 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs6906662 | 0.882 | 0.200 | 6 | 32298729 | intron variant | G/A | snv | 6.8E-02 | 6 | ||
rs241448 | 0.882 | 0.200 | 6 | 32828908 | stop lost | A/G | snv | 0.32 | 0.27 | 5 | |
rs241453 | 0.882 | 0.160 | 6 | 32828449 | 3 prime UTR variant | G/A | snv | 0.25 | 5 | ||
rs2517459 | 0.882 | 0.160 | 6 | 30929245 | downstream gene variant | T/C | snv | 0.74 | 5 | ||
rs8192591 | 0.882 | 0.160 | 6 | 32218019 | missense variant | C/T | snv | 2.5E-02 | 2.2E-02 | 5 | |
rs9469003 | 0.882 | 0.160 | 6 | 31440051 | intron variant | T/C | snv | 0.22 | 5 | ||
rs8283 | 0.882 | 0.120 | 6 | 32115523 | 3 prime UTR variant | A/G | snv | 0.25 | 4 | ||
rs9391734 | 0.882 | 0.160 | 6 | 32130206 | 5 prime UTR variant | G/A | snv | 0.11 | 4 |