Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs979614 | 1.000 | 0.080 | 6 | 20661892 | intron variant | A/G | snv | 0.35 | 1 | ||
rs9688952 | 1.000 | 0.080 | 6 | 20741152 | intron variant | G/A | snv | 0.38 | 1 | ||
rs9465871 | 0.882 | 0.120 | 6 | 20717024 | intron variant | T/C | snv | 0.30 | 3 | ||
rs9465852 | 1.000 | 0.080 | 6 | 20641669 | intron variant | G/A;C | snv | 1 | |||
rs9465850 | 1.000 | 0.080 | 6 | 20639178 | intron variant | C/T | snv | 0.19 | 1 | ||
rs9465847 | 1.000 | 0.080 | 6 | 20634197 | intron variant | G/T | snv | 0.19 | 1 | ||
rs9465846 | 1.000 | 0.080 | 6 | 20634110 | intron variant | C/T | snv | 0.19 | 1 | ||
rs9460550 | 1.000 | 0.080 | 6 | 20719330 | intron variant | G/A | snv | 0.30 | 1 | ||
rs9460546 | 1.000 | 0.080 | 6 | 20663401 | intron variant | T/G | snv | 0.40 | 1 | ||
rs9460545 | 1.000 | 0.080 | 6 | 20661319 | intron variant | T/A;C | snv | 1 | |||
rs9460544 | 1.000 | 0.080 | 6 | 20661298 | intron variant | G/A;T | snv | 1 | |||
rs9460540 | 1.000 | 0.080 | 6 | 20648531 | intron variant | A/G | snv | 0.35 | 1 | ||
rs9460538 | 1.000 | 0.080 | 6 | 20640306 | intron variant | G/A | snv | 0.70 | 1 | ||
rs9368226 | 1.000 | 0.080 | 6 | 20722826 | intron variant | T/C | snv | 0.29 | 1 | ||
rs9368224 | 1.000 | 0.080 | 6 | 20719001 | intron variant | T/A | snv | 0.30 | 1 | ||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 5 | |||
rs9368219 | 1.000 | 0.080 | 6 | 20674460 | intron variant | C/T | snv | 0.19 | 3 | ||
rs9368216 | 1.000 | 0.080 | 6 | 20654879 | intron variant | A/C;G | snv | 1 | |||
rs9358358 | 1.000 | 0.080 | 6 | 20719162 | intron variant | A/C | snv | 0.19 | 1 | ||
rs9358357 | 1.000 | 0.080 | 6 | 20718914 | intron variant | A/G | snv | 0.30 | 1 | ||
rs9358356 | 1.000 | 0.080 | 6 | 20667151 | intron variant | T/C | snv | 0.39 | 1 | ||
rs9358355 | 1.000 | 0.080 | 6 | 20654666 | intron variant | T/C | snv | 0.27 | 1 | ||
rs9356748 | 1.000 | 0.080 | 6 | 20724866 | intron variant | T/A | snv | 0.14 | 1 | ||
rs9356747 | 1.000 | 0.080 | 6 | 20724776 | intron variant | T/A | snv | 0.35 | 1 | ||
rs9356746 | 1.000 | 0.080 | 6 | 20720048 | intron variant | T/C | snv | 0.15 | 1 |