Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4676410 | 0.716 | 0.240 | 2 | 240624322 | intron variant | G/A | snv | 0.26 | 17 | ||
rs3749171 | 0.807 | 0.120 | 2 | 240630275 | missense variant | C/T | snv | 0.16; 9.4E-06 | 0.19 | 6 | |
rs34236350 | 2 | 240628909 | 5 prime UTR variant | C/T | snv | 0.25 | 2 | ||||
rs3749172 | 1.000 | 0.040 | 2 | 240630832 | missense variant | A/C;T | snv | 0.56; 2.0E-05 | 1 |