Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 8 | |||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 7 | |
rs8042374 | 0.807 | 0.200 | 15 | 78615690 | intron variant | A/G | snv | 0.29 | 4 | ||
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 3 | |
rs578776 | 0.742 | 0.240 | 15 | 78596058 | 3 prime UTR variant | G/A | snv | 0.39 | 3 | ||
rs938682 | 0.851 | 0.080 | 15 | 78604205 | intron variant | G/A | snv | 0.72 | 3 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 3 | |||
rs6495309 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 3 | |||
rs7177514 | 0.882 | 0.080 | 15 | 78615064 | intron variant | C/G;T | snv | 1 | |||
rs4887069 | 15 | 78616728 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs8042059 | 0.882 | 0.080 | 15 | 78615517 | intron variant | A/C;T | snv | 1 | |||
rs3743078 | 0.807 | 0.160 | 15 | 78602417 | intron variant | C/A;G | snv | 1 | |||
rs1317286 | 0.925 | 0.120 | 15 | 78603787 | intron variant | A/G | snv | 0.30 | 1 | ||
rs3743075 | 1.000 | 0.040 | 15 | 78617110 | missense variant | T/A;C | snv | 4.0E-06; 0.66 | 1 | ||
rs11637630 | 0.882 | 0.080 | 15 | 78607377 | intron variant | G/A | snv | 0.71 | 1 | ||
rs12443170 | 1.000 | 0.040 | 15 | 78615394 | intron variant | G/A | snv | 0.12 | 1 | ||
rs6495308 | 0.851 | 0.160 | 15 | 78615314 | intron variant | T/C | snv | 0.29 | 1 |