Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs3789243 | 0.776 | 0.120 | 7 | 87591570 | intron variant | A/G | snv | 0.50 | 14 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1202168 | 1.000 | 0.080 | 7 | 87566646 | intron variant | G/A | snv | 0.39 | 1 | ||
rs979090956 | 0.827 | 0.200 | 7 | 87553822 | missense variant | G/C | snv | 5 | |||
rs868755 | 1.000 | 0.080 | 7 | 87560614 | intron variant | T/G | snv | 0.68 | 1 |