Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1040558 | 1.000 | 0.080 | 6 | 20713475 | intron variant | A/G | snv | 0.19 | 1 | ||
rs10440833 | 1.000 | 0.080 | 6 | 20687890 | intron variant | T/A;G | snv | 0.26 | 1 | ||
rs10946398 | 0.827 | 0.160 | 6 | 20660803 | intron variant | A/C | snv | 0.40 | 3 | ||
rs10946403 | 1.000 | 0.080 | 6 | 20717173 | intron variant | A/G | snv | 0.30 | 1 | ||
rs10946406 | 1.000 | 0.080 | 6 | 20758529 | intron variant | A/G;T | snv | 1 | |||
rs11753081 | 1.000 | 0.080 | 6 | 20705359 | intron variant | T/G | snv | 0.19 | 1 | ||
rs12111351 | 1.000 | 0.080 | 6 | 20724327 | intron variant | T/G | snv | 0.34 | 1 | ||
rs12664021 | 1.000 | 0.080 | 6 | 20760849 | intron variant | C/T | snv | 0.11 | 1 | ||
rs145494032 | 1.000 | 0.080 | 6 | 20665715 | intron variant | -/C | delins | 4.9E-05 | 1 | ||
rs1569699 | 1.000 | 0.080 | 6 | 20679079 | intron variant | T/G | snv | 0.41 | 1 | ||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 3 | ||
rs2328529 | 1.000 | 0.080 | 6 | 20631722 | intron variant | C/A | snv | 0.19 | 1 | ||
rs2328531 | 1.000 | 0.080 | 6 | 20643521 | intron variant | A/G;T | snv | 1 | |||
rs2328545 | 1.000 | 0.080 | 6 | 20653319 | intron variant | G/A;C | snv | 1 | |||
rs2328548 | 1.000 | 0.080 | 6 | 20716727 | intron variant | G/A;T | snv | 1 | |||
rs2820001 | 1.000 | 0.080 | 6 | 20758712 | intron variant | G/T | snv | 0.85 | 1 | ||
rs4235999 | 1.000 | 0.080 | 6 | 20642991 | intron variant | C/G;T | snv | 0.39 | 1 | ||
rs4493738 | 1.000 | 0.080 | 6 | 20775429 | intron variant | A/G | snv | 7.5E-02 | 1 | ||
rs4710938 | 1.000 | 0.080 | 6 | 20640673 | intron variant | A/G | snv | 0.42 | 1 | ||
rs4710939 | 1.000 | 0.080 | 6 | 20644713 | intron variant | A/G | snv | 0.41 | 1 | ||
rs4710940 | 1.000 | 0.080 | 6 | 20657781 | intron variant | A/C | snv | 0.46 | 1 | ||
rs4712522 | 1.000 | 0.080 | 6 | 20656569 | intron variant | C/G | snv | 0.40 | 1 | ||
rs4712523 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 3 | ||
rs4712524 | 0.925 | 0.120 | 6 | 20657634 | intron variant | A/G | snv | 0.40 | 2 | ||
rs4712525 | 1.000 | 0.080 | 6 | 20662735 | intron variant | C/G;T | snv | 1 |