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 | ||
rs1057519949 | 0.851 | 0.120 | 7 | 151490964 | missense variant | A/T | snv | 6 | |||
rs718314 | 0.882 | 0.120 | 12 | 26300350 | intron variant | A/G | snv | 0.27 | 6 | ||
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 | ||
rs2228230 | 0.882 | 0.120 | 4 | 54285873 | synonymous variant | C/A;T | snv | 4.0E-06; 0.18 | 5 | ||
rs7105934 | 0.827 | 0.120 | 11 | 69424973 | upstream gene variant | G/A;C | snv | 5 | |||
rs786202724 | 0.925 | 0.120 | 7 | 116777403 | missense variant | G/A | snv | 7.0E-06 | 5 | ||
rs121913668 | 0.882 | 0.120 | 7 | 116778827 | missense variant | T/C | snv | 4 | |||
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 | |||
rs786205165 | 0.882 | 0.120 | 1 | 11157173 | missense variant | C/A;T | snv | 4 | |||
rs1057519913 | 0.925 | 0.120 | 1 | 11157172 | missense variant | G/C | snv | 3 | |||
rs1060502375 | 0.882 | 0.120 | 17 | 17228023 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
rs1131690838 | 0.925 | 0.120 | 17 | 17228135 | frameshift variant | C/- | del | 3 | |||
rs11894252 | 0.925 | 0.120 | 2 | 46306237 | intron variant | T/A;C;G | snv | 3 | |||
rs121913670 | 0.925 | 0.120 | 7 | 116783329 | missense variant | G/A | snv | 3 | |||
rs121913673 | 0.925 | 0.120 | 7 | 116782048 | missense variant | C/G;T | snv | 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 | |||
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 |