Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35261542 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 3 | ||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 3 | |||
rs35612982 | 1.000 | 0.080 | 6 | 20682391 | intron variant | T/C | snv | 0.29 | 2 | ||
rs6931514 | 0.925 | 0.120 | 6 | 20703721 | intron variant | A/G | snv | 0.27 | 2 | ||
rs742642 | 1.000 | 0.080 | 6 | 20664850 | intron variant | G/A | snv | 0.21 | 2 | ||
rs7754840 | 0.807 | 0.200 | 6 | 20661019 | intron variant | G/A;C;T | snv | 2 | |||
rs9356744 | 0.882 | 0.120 | 6 | 20685255 | intron variant | T/C | snv | 0.42 | 2 | ||
rs9358356 | 1.000 | 0.080 | 6 | 20667151 | intron variant | T/C | snv | 0.39 | 2 | ||
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 | 1 | ||
rs2206734 | 0.882 | 0.160 | 6 | 20694653 | intron variant | C/T | snv | 0.20 | 1 | ||
rs4712523 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 1 | ||
rs4712524 | 0.925 | 0.120 | 6 | 20657634 | intron variant | A/G | snv | 0.40 | 1 | ||
rs6908425 | 0.752 | 0.320 | 6 | 20728500 | intron variant | T/C | snv | 0.78 | 1 | ||
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 1 | |||
rs7766070 | 1.000 | 0.080 | 6 | 20686342 | intron variant | C/A | snv | 0.25 | 1 | ||
rs9348440 | 1.000 | 0.080 | 6 | 20641105 | intron variant | C/T | snv | 0.13 | 1 | ||
rs9460550 | 1.000 | 0.080 | 6 | 20719330 | intron variant | G/A | snv | 0.30 | 1 | ||
rs9465871 | 0.882 | 0.120 | 6 | 20717024 | intron variant | T/C | snv | 0.30 | 1 |