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 | |
rs20417 | 0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv | 57 | |||
rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 46 | ||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
rs2200733 | 0.752 | 0.240 | 4 | 110789013 | intergenic variant | C/T | snv | 0.18 | 12 | ||
rs5065 | 0.763 | 0.240 | 1 | 11846011 | stop lost | A/G | snv | 0.14 | 0.21 | 12 | |
rs1800779 | 0.763 | 0.320 | 7 | 150992855 | intron variant | G/A;C | snv | 9 | |||
rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 8 | ||
rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 7 | |||
rs1906591 | 0.851 | 0.200 | 4 | 110787733 | intergenic variant | G/A | snv | 0.15 | 5 | ||
rs761740955 | 0.827 | 0.200 | 4 | 154566637 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs13143308 | 0.882 | 0.120 | 4 | 110793263 | upstream gene variant | T/C;G | snv | 4 | |||
rs2910829 | 0.925 | 0.080 | 5 | 60174072 | intron variant | G/A | snv | 0.52 | 3 | ||
rs152312 | 0.925 | 0.080 | 5 | 60491989 | non coding transcript exon variant | G/A;T | snv | 3 | |||
rs12932445 | 0.925 | 0.080 | 16 | 73035989 | intron variant | T/C | snv | 0.18 | 3 | ||
rs6891174 | 0.925 | 0.040 | 5 | 173213587 | intergenic variant | A/G | snv | 0.73 | 2 | ||
rs5067 | 0.925 | 0.080 | 1 | 11845924 | 3 prime UTR variant | A/G;T | snv | 0.21 | 2 | ||
rs1003346 | 1.000 | 9 | 109053060 | intron variant | C/A | snv | 0.43 | 2 | |||
rs16939239 | 1.000 | 8 | 76122993 | intergenic variant | G/A | snv | 0.14 | 1 | |||
rs638704 | 1.000 | 1 | 170629046 | intron variant | C/T | snv | 0.64 | 1 | |||
rs2257073 | 1.000 | 7 | 151186200 | intron variant | C/T | snv | 0.26 | 1 | |||
rs4727833 | 1.000 | 7 | 116507854 | 3 prime UTR variant | C/G;T | snv | 1 | ||||
rs11596587 | 1.000 | 10 | 69354232 | intron variant | C/T | snv | 0.11 | 1 | |||
rs2273235 | 1.000 | 5 | 150527971 | synonymous variant | T/G | snv | 0.45 | 0.42 | 1 |