Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs937475913 | 0.790 | 0.120 | 8 | 47936435 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
rs7859384 | 0.882 | 0.120 | 9 | 79507370 | intron variant | A/C;G | snv | 6 | |||
rs1049380 | 0.827 | 0.120 | 12 | 26336611 | 3 prime UTR variant | G/T | snv | 0.69 | 5 | ||
rs7105934 | 0.827 | 0.120 | 11 | 69424973 | upstream gene variant | G/A;C | snv | 5 | |||
rs1312268347 | 0.925 | 0.120 | 9 | 133734172 | start lost | A/G | snv | 5.0E-06 | 4 | ||
rs141683432 | 0.882 | 0.120 | 19 | 38287929 | missense variant | C/T | snv | 1.6E-03 | 1.9E-03 | 4 | |
rs779805 | 0.851 | 0.120 | 3 | 10141653 | 5 prime UTR variant | G/A;C | snv | 4 | |||
rs1060502375 | 0.882 | 0.120 | 17 | 17228023 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
rs1362888828 | 0.925 | 0.120 | 21 | 31266532 | synonymous variant | C/T | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs553863637 | 0.925 | 0.120 | 2 | 68382602 | missense variant | G/A;C | snv | 4.8E-05 | 3 | ||
rs611646 | 0.882 | 0.120 | 11 | 108306370 | intron variant | T/A;C | snv | 3 | |||
rs718314 | 0.882 | 0.120 | 12 | 26300350 | intron variant | A/G | snv | 0.27 | 3 | ||
rs776399733 | 0.882 | 0.120 | 3 | 10141965 | missense variant | C/A;T | snv | 6.5E-06 | 3 | ||
rs1010980331 | 0.925 | 0.120 | 17 | 17215072 | missense variant | T/C | snv | 2 | |||
rs10771279 | 0.925 | 0.120 | 12 | 26377610 | intron variant | T/A;C | snv | 0.40 | 2 | ||
rs1131690838 | 0.925 | 0.120 | 17 | 17228135 | frameshift variant | C/- | del | 2 | |||
rs1154454 | 0.925 | 0.120 | 4 | 99417185 | intron variant | A/G | snv | 0.22 | 2 | ||
rs11762213 | 0.925 | 0.120 | 7 | 116699228 | synonymous variant | G/A | snv | 3.3E-02 | 3.3E-02 | 2 | |
rs11813268 | 0.925 | 0.120 | 10 | 103922538 | upstream gene variant | C/T | snv | 0.31 | 2 | ||
rs11894252 | 0.925 | 0.120 | 2 | 46306237 | intron variant | T/A;C;G | snv | 2 | |||
rs1259293 | 0.925 | 0.120 | 3 | 120421014 | intron variant | T/C | snv | 0.59 | 2 | ||
rs12617313 | 0.925 | 0.120 | 2 | 46332637 | intron variant | A/G;T | snv | 2 | |||
rs1417080 | 0.925 | 0.120 | 9 | 79515946 | non coding transcript exon variant | T/C | snv | 0.35 | 2 | ||
rs1449964136 | 0.925 | 0.120 | 3 | 69936725 | start lost | G/A | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs1802074 | 0.925 | 0.120 | 7 | 37907501 | missense variant | C/T | snv | 0.20 | 0.24 | 2 |