Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs1057519743 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 6 | |||
rs4958351 | 0.882 | 0.120 | 5 | 153790814 | intron variant | G/A;T | snv | 0.31 | 3 |