Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9277341 | 0.882 | 0.280 | 6 | 33071848 | intron variant | T/A;C | snv | 3 | |||
rs3077 | 0.701 | 0.440 | 6 | 33065245 | 3 prime UTR variant | A/G | snv | 0.29 | 3 | ||
rs987870 | 0.851 | 0.160 | 6 | 33075103 | intron variant | A/G | snv | 0.19 | 3 | ||
rs9277359 | 0.925 | 0.200 | 6 | 33082247 | intron variant | C/A;T | snv | 2 | |||
rs9277378 | 0.827 | 0.320 | 6 | 33082502 | intron variant | A/G | snv | 0.40 | 2 | ||
rs928976 | 0.925 | 0.200 | 6 | 33081434 | intron variant | C/T | snv | 0.41 | 2 | ||
rs1431403 | 0.925 | 0.200 | 6 | 33079254 | intron variant | T/C | snv | 0.37 | 2 | ||
rs7770370 | 0.925 | 0.160 | 6 | 33081144 | non coding transcript exon variant | A/G | snv | 0.27 | 2 | ||
rs1367728 | 1.000 | 0.120 | 6 | 33067038 | non coding transcript exon variant | G/A | snv | 0.10 | 1 | ||
rs1126542 | 1.000 | 0.080 | 6 | 33069647 | missense variant | T/A;C;G | snv | 0.24 | 0.28 | 1 | |
rs17214519 | 1.000 | 0.080 | 6 | 33064411 | downstream gene variant | G/A;T | snv | 1 | |||
rs2301220 | 1.000 | 0.080 | 6 | 33070989 | intron variant | C/A;T | snv | 1 | |||
rs1431401 | 1.000 | 0.080 | 6 | 33073409 | intron variant | G/A | snv | 0.29 | 1 | ||
rs6914995 | 1.000 | 0.080 | 6 | 33072967 | intron variant | G/C | snv | 0.29 | 1 | ||
rs3830066 | 1.000 | 0.080 | 6 | 33069410 | non coding transcript exon variant | C/A;G | snv | 1 | |||
rs9469341 | 1.000 | 0.080 | 6 | 33068100 | 3 prime UTR variant | A/C;G | snv | 1 | |||
rs9348904 | 1.000 | 0.080 | 6 | 33073058 | intron variant | A/G | snv | 0.29 | 1 | ||
rs2301224 | 1.000 | 0.080 | 6 | 33070592 | intron variant | C/A | snv | 0.28 | 1 | ||
rs10214910 | 1.000 | 0.080 | 6 | 33069898 | intron variant | C/A | snv | 0.23 | 0.32 | 1 | |
rs9469332 | 1.000 | 0.080 | 6 | 33067099 | non coding transcript exon variant | T/A;C | snv | 1 | |||
rs1431400 | 1.000 | 0.080 | 6 | 33073399 | intron variant | C/T | snv | 0.29 | 1 | ||
rs9469331 | 1.000 | 0.080 | 6 | 33067008 | non coding transcript exon variant | G/A | snv | 0.32 | 1 | ||
rs4640928 | 1.000 | 0.080 | 6 | 33072819 | intron variant | A/G | snv | 0.29 | 1 | ||
rs2308911 | 1.000 | 0.080 | 6 | 33069803 | missense variant | T/G | snv | 0.23 | 0.28 | 1 | |
rs1431399 | 1.000 | 0.080 | 6 | 33073257 | intron variant | A/G;T | snv | 1 |