Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 30 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 10 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 8 | ||
rs157582 | 0.851 | 0.160 | 19 | 44892962 | intron variant | C/T | snv | 0.24 | 0.29 | 5 | |
rs117905930 | 1.000 | 0.080 | 9 | 88973603 | intron variant | C/A;T | snv | 2 | |||
rs147906088 | 1.000 | 0.080 | 7 | 54496119 | intergenic variant | C/A;T | snv | 2 | |||
rs56214552 | 1.000 | 0.080 | 8 | 93011994 | intron variant | T/G | snv | 0.24 | 2 | ||
rs62187521 | 1.000 | 0.080 | 20 | 959154 | 3 prime UTR variant | C/T | snv | 4.8E-03 | 2 | ||
rs6479525 | 1.000 | 0.080 | 9 | 90331096 | intron variant | G/A | snv | 0.44 | 2 | ||
rs72639058 | 1.000 | 0.080 | 1 | 13913797 | intron variant | C/A;T | snv | 2 |