Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 12 | ||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 10 | ||
rs389884 | 0.776 | 0.440 | 6 | 31973120 | non coding transcript exon variant | A/G | snv | 7.1E-02 | 7 | ||
rs1980493 | 0.776 | 0.400 | 6 | 32395438 | intron variant | T/C | snv | 0.13 | 6 | ||
rs3115663 | 0.827 | 0.360 | 6 | 31634066 | non coding transcript exon variant | T/C | snv | 0.17 | 6 | ||
rs3130544 | 0.807 | 0.360 | 6 | 31090563 | intergenic variant | C/A | snv | 7.4E-02 | 6 | ||
rs3130564 | 0.790 | 0.360 | 6 | 31133897 | intron variant | C/T | snv | 0.14 | 5 | ||
rs1480380 | 0.763 | 0.360 | 6 | 32945469 | intron variant | C/T | snv | 0.11 | 4 | ||
rs3129939 | 0.827 | 0.360 | 6 | 32368989 | intron variant | A/G | snv | 0.14 | 4 | ||
rs2233956 | 0.827 | 0.320 | 6 | 31113428 | upstream gene variant | T/C | snv | 0.12 | 3 | ||
rs3134792 | 0.851 | 0.280 | 6 | 31344549 | intron variant | T/G | snv | 8.8E-02 | 3 | ||
rs3134945 | 0.827 | 0.240 | 6 | 32178715 | intron variant | C/A | snv | 0.18 | 3 | ||
rs1265159 | 0.882 | 0.240 | 6 | 31172270 | intron variant | G/A | snv | 0.21 | 2 | ||
rs4664308 | 0.851 | 0.160 | 2 | 160060986 | intron variant | A/G | snv | 0.30 | 1 | ||
rs3130618 | 0.827 | 0.360 | 6 | 31664357 | missense variant | C/A;T | snv | 0.15; 4.0E-06 | 6 | ||
rs7775397 | 0.790 | 0.400 | 6 | 32293475 | missense variant | T/G | snv | 6.0E-02 | 6.4E-02 | 6 | |
rs7750641 | 0.807 | 0.360 | 6 | 31161533 | missense variant | C/T | snv | 7.0E-02 | 7.6E-02 | 5 | |
rs3132580 | 0.790 | 0.360 | 6 | 30952347 | missense variant | G/A | snv | 8.0E-02 | 9.3E-02 | 6 | |
rs3096697 | 0.882 | 0.200 | 6 | 32166733 | missense variant | G/A | snv | 0.16 | 0.18 | 2 | |
rs652888 | 0.776 | 0.480 | 6 | 31883457 | non coding transcript exon variant | A/G | snv | 0.18 | 0.20 | 6 |