Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs821616 | 0.752 | 0.200 | 1 | 232008852 | missense variant | A/T | snv | 0.26 | 0.29 | 13 | |
rs4650608 | 0.851 | 0.040 | 1 | 78772330 | intergenic variant | T/C | snv | 0.29 | 7 | ||
rs5177 | 0.851 | 0.120 | 1 | 53246063 | 3 prime UTR variant | G/A;C | snv | 6 | |||
rs4949526 | 1.000 | 0.040 | 1 | 29959372 | intergenic variant | T/C | snv | 0.54 | 3 | ||
rs1009080 | 1 | 29958713 | intergenic variant | G/A | snv | 0.54 | 2 | ||||
rs11164835 | 1 | 92913536 | intron variant | G/A | snv | 0.35 | 2 | ||||
rs12745968 | 1 | 92936280 | intron variant | A/G | snv | 0.36 | 2 | ||||
rs771065515 | 1 | 156115240 | missense variant | A/G | snv | 2.5E-05 | 7.0E-06 | 2 | |||
rs144851946 | 1 | 156138701 | missense variant | G/A;T | snv | 1.4E-04; 4.0E-06 | 1 | ||||
rs373584456 | 1 | 156136335 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |||
rs374726751 | 1 | 156136245 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |||
rs374926367 | 1 | 156139089 | missense variant | A/G | snv | 1.2E-04 | 1.0E-04 | 1 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs3771829 | 0.790 | 0.120 | 2 | 75137019 | intron variant | C/G | snv | 0.11 | 9 | ||
rs121918805 | 0.925 | 0.080 | 2 | 166002660 | missense variant | C/A;T | snv | 2.0E-05 | 4 | ||
rs4675690 | 2 | 207643083 | intergenic variant | C/T | snv | 0.48 | 3 | ||||
rs10496702 | 2 | 133247997 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs7600871 | 2 | 133257389 | intron variant | C/T | snv | 0.16 | 2 | ||||
rs6280 | 0.602 | 0.520 | 3 | 114171968 | missense variant | C/T | snv | 0.63 | 0.54 | 57 | |
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 |