Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs4648068 | 0.790 | 0.240 | 4 | 102597148 | intron variant | A/G | snv | 0.31 | 9 | ||
rs3774937 | 0.776 | 0.280 | 4 | 102513096 | intron variant | T/C | snv | 0.26 | 4 | ||
rs1598859 | 0.925 | 0.080 | 4 | 102585287 | intron variant | T/C | snv | 0.34 | 4 | ||
rs3774934 | 0.851 | 0.080 | 4 | 102506319 | intron variant | A/C;G;T | snv | 4 | |||
rs230530 | 0.882 | 0.080 | 4 | 102532823 | intron variant | A/G | snv | 0.37 | 4 | ||
rs230521 | 0.851 | 0.160 | 4 | 102542171 | intron variant | C/G | snv | 0.59 | 4 | ||
rs147574894 | 0.925 | 0.080 | 4 | 102600911 | missense variant | A/G | snv | 9.6E-05 | 3.9E-04 | 4 | |
rs3774968 | 0.882 | 0.120 | 4 | 102609955 | intron variant | A/G | snv | 0.64 | 4 | ||
rs774062108 | 0.925 | 0.240 | 4 | 102607651 | splice region variant | T/G | snv | 4.0E-06 | 3 | ||
rs4648127 | 0.882 | 0.080 | 4 | 102614748 | intron variant | C/T | snv | 4.3E-02 | 3 | ||
rs72696119 | 0.925 | 0.120 | 4 | 102501347 | 5 prime UTR variant | C/G | snv | 0.43 | 3 | ||
rs230525 | 0.882 | 0.080 | 4 | 102537720 | non coding transcript exon variant | G/A | snv | 0.69 | 3 | ||
rs230496 | 0.882 | 0.080 | 4 | 102567334 | intron variant | G/A | snv | 0.59 | 3 | ||
rs13117745 | 0.882 | 0.080 | 4 | 102557546 | intron variant | C/T | snv | 0.18 | 3 | ||
rs230541 | 0.882 | 0.080 | 4 | 102576628 | intron variant | G/A | snv | 0.58 | 3 | ||
rs1801 | 0.882 | 0.080 | 4 | 102579897 | intron variant | C/G;T | snv | 3 | |||
rs4648110 | 0.925 | 0.080 | 4 | 102612664 | intron variant | T/A | snv | 0.22 | 3 | ||
rs4648143 | 1.000 | 0.080 | 4 | 102616617 | 3 prime UTR variant | G/A;T | snv | 5.0E-03; 4.0E-06 | 2 | ||
rs1241312324 | 0.925 | 0.200 | 4 | 102567083 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs1020760 | 0.925 | 0.040 | 4 | 102593288 | non coding transcript exon variant | C/G | snv | 0.42 | 2 | ||
rs764911742 | 4 | 102606567 | synonymous variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |||
rs1609798 | 1.000 | 0.040 | 4 | 102616285 | intron variant | C/T | snv | 0.26 | 1 | ||
rs28720239 | 1.000 | 0.080 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 1 | |||
rs3774932 | 1.000 | 0.080 | 4 | 102503036 | intron variant | A/G;T | snv | 1 |