Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
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 | ||
rs4712525 | 1.000 | 0.080 | 6 | 20662735 | intron variant | C/G;T | snv | 1 | |||
rs4712526 | 1.000 | 0.080 | 6 | 20662804 | intron variant | T/A | snv | 0.40 | 1 | ||
rs6456364 | 1.000 | 0.080 | 6 | 20649023 | intron variant | A/T | snv | 0.13 | 1 | ||
rs6456367 | 1.000 | 0.080 | 6 | 20659356 | intron variant | T/A | snv | 0.40 | 1 | ||
rs6456369 | 1.000 | 0.080 | 6 | 20660134 | intron variant | T/A;C;G | snv | 1 | |||
rs6906327 | 1.000 | 0.080 | 6 | 20659228 | intron variant | G/A | snv | 0.47 | 1 | ||
rs6909558 | 1.000 | 0.080 | 6 | 20759946 | intron variant | C/T | snv | 0.11 | 1 | ||
rs6925328 | 1.000 | 0.080 | 6 | 20642554 | intron variant | A/G | snv | 0.71 | 1 | ||
rs6928012 | 1.000 | 0.080 | 6 | 20728282 | intron variant | C/T | snv | 0.49 | 1 | ||
rs6935599 | 1.000 | 0.080 | 6 | 20716864 | intron variant | A/G | snv | 0.31 | 1 | ||
rs6940200 | 1.000 | 0.080 | 6 | 20635031 | intron variant | C/T | snv | 0.19 | 1 | ||
rs742642 | 1.000 | 0.080 | 6 | 20664850 | intron variant | G/A | snv | 0.21 | 1 | ||
rs7452218 | 1.000 | 0.080 | 6 | 20767240 | intron variant | C/T | snv | 0.11 | 1 | ||
rs7747752 | 1.000 | 0.080 | 6 | 20725192 | intron variant | G/C | snv | 0.34 | 1 | ||
rs7748382 | 1.000 | 0.080 | 6 | 20665318 | intron variant | G/A | snv | 0.41 | 1 |