Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10895068 | 0.752 | 0.240 | 11 | 101129483 | 5 prime UTR variant | C/T | snv | 3.6E-02 | 14 | ||
rs1408080623 | 0.851 | 0.080 | 11 | 101128058 | missense variant | G/A | snv | 5 | |||
rs750042441 | 0.827 | 0.160 | 11 | 101128367 | missense variant | G/A;C | snv | 6.1E-05; 4.3E-06 | 5 | ||
rs776880789 | 0.925 | 0.080 | 11 | 101128241 | missense variant | G/C;T | snv | 4.7E-06; 4.7E-06 | 4 | ||
rs761872690 | 0.925 | 0.080 | 11 | 101128246 | synonymous variant | G/A | snv | 2.8E-05 | 3 | ||
rs3740753 | 0.925 | 0.080 | 11 | 101128040 | missense variant | C/G | snv | 0.13 | 0.12 | 2 | |
rs376101426 | 0.925 | 0.080 | 11 | 101128556 | missense variant | A/G | snv | 1.4E-05 | 2.8E-05 | 2 | |
rs757679709 | 0.925 | 0.080 | 11 | 101129045 | missense variant | G/A;C | snv | 3.0E-05 | 2 | ||
rs772873062 | 0.925 | 0.080 | 11 | 101128998 | missense variant | A/G | snv | 4.8E-06 | 2 | ||
rs11571149 | 0.925 | 0.080 | 11 | 101127937 | missense variant | G/T | snv | 2 | |||
rs1312187959 | 0.925 | 0.080 | 11 | 101128554 | missense variant | C/T | snv | 1.4E-05 | 7.0E-06 | 2 | |
rs518162 | 0.925 | 0.080 | 11 | 101129770 | 5 prime UTR variant | A/G | snv | 0.86 | 2 | ||
rs775092033 | 0.925 | 0.080 | 11 | 101127471 | missense variant | G/C | snv | 2 |