Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
rs1799977 | 0.662 | 0.440 | 3 | 37012077 | missense variant | A/C;G;T | snv | 0.23 | 28 | ||
rs876658657 | 0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 | 25 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs352139 | 0.732 | 0.320 | 3 | 52224356 | intron variant | T/C | snv | 0.51 | 0.54 | 18 | |
rs1418586322 | 0.827 | 0.160 | 3 | 37050495 | missense variant | C/G | snv | 4.0E-06 | 6 | ||
rs2270916 | 0.851 | 0.120 | 3 | 122282252 | intron variant | T/C | snv | 0.13 | 0.11 | 6 | |
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 4 | ||
rs10934578 | 0.925 | 0.080 | 3 | 122258435 | intron variant | G/T | snv | 0.30 | 4 | ||
rs756363791 | 0.882 | 0.080 | 3 | 9756823 | missense variant | G/A | snv | 2.0E-05 | 4 | ||
rs352144 | 0.925 | 0.080 | 3 | 52227452 | intron variant | T/G | snv | 3.7E-02 | 3 | ||
rs63751701 | 0.925 | 0.080 | 3 | 36993663 | stop gained | G/A;T | snv | 3 | |||
rs760891242 | 0.925 | 0.080 | 3 | 14168309 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs9869263 | 0.925 | 0.080 | 3 | 190312891 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.83; 4.0E-06 | 3 | ||
rs11923427 | 0.925 | 0.080 | 3 | 12622336 | intron variant | C/G;T | snv | 2 | |||
rs12485716 | 0.925 | 0.080 | 3 | 122260843 | intron variant | G/A | snv | 0.36 | 2 | ||
rs12490683 | 0.925 | 0.080 | 3 | 75329934 | non coding transcript exon variant | G/A | snv | 0.46 | 2 | ||
rs12497343 | 0.925 | 0.080 | 3 | 75330074 | intron variant | C/G;T | snv | 2 | |||
rs17250717 | 0.925 | 0.080 | 3 | 122261339 | intron variant | G/T | snv | 7.4E-02 | 2 | ||
rs1802757 | 0.925 | 0.080 | 3 | 122286284 | 3 prime UTR variant | C/T | snv | 0.17 | 2 | ||
rs3804592 | 0.925 | 0.080 | 3 | 122260382 | intron variant | G/A | snv | 0.18 | 2 | ||
rs4678174 | 0.925 | 0.080 | 3 | 122282024 | intron variant | C/T | snv | 0.56 | 2 | ||
rs779795819 | 0.925 | 0.080 | 3 | 37048526 | frameshift variant | -/ATTG | delins | 4.0E-06 | 2 | ||
rs876658198 | 0.925 | 0.080 | 3 | 37028855 | missense variant | G/A | snv | 2 | |||
rs3804099 | 0.627 | 0.680 | 4 | 153703504 | synonymous variant | T/C | snv | 0.40 | 0.48 | 40 |