Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3025035 | 0.851 | 0.240 | 6 | 43783622 | non coding transcript exon variant | C/T | snv | 0.14 | 4 | ||
rs3025036 | 1.000 | 0.080 | 6 | 43783932 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
rs1479430148 | 1.000 | 0.120 | 6 | 43784861 | 3 prime UTR variant | A/T | snv | 1 | |||
rs3025040 | 0.882 | 0.120 | 6 | 43785314 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs3025053 | 0.925 | 0.120 | 6 | 43785588 | 3 prime UTR variant | G/A | snv | 8.6E-02 | 2 |