Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 1 | ||
rs10789230 | 1.000 | 0.040 | 1 | 67264945 | downstream gene variant | G/C;T | snv | 1 | |||
rs10801047 | 1.000 | 0.040 | 1 | 191590226 | intergenic variant | A/T | snv | 0.82 | 1 | ||
rs10889676 | 0.827 | 0.120 | 1 | 67256884 | intron variant | C/A;T | snv | 1 | |||
rs11208994 | 1.000 | 0.040 | 1 | 67059360 | regulatory region variant | A/G;T | snv | 1 | |||
rs11209002 | 1.000 | 0.040 | 1 | 67124778 | intron variant | T/C | snv | 0.77 | 1 | ||
rs11209003 | 1.000 | 0.040 | 1 | 67135449 | intron variant | G/T | snv | 0.28 | 1 | ||
rs11209008 | 0.882 | 0.080 | 1 | 67157615 | intron variant | G/A;T | snv | 5.7E-02 | 1 | ||
rs11209032 | 0.752 | 0.400 | 1 | 67274409 | upstream gene variant | G/A | snv | 0.30 | 1 | ||
rs11265519 | 1.000 | 0.040 | 1 | 160909123 | intergenic variant | C/A | snv | 0.60 | 1 | ||
rs1142287 | 1.000 | 0.040 | 1 | 155260340 | synonymous variant | C/T | snv | 0.34 | 0.36 | 1 | |
rs11465802 | 1.000 | 0.040 | 1 | 67219915 | intron variant | A/C;T | snv | 1 | |||
rs11804284 | 1.000 | 0.040 | 1 | 67233571 | intron variant | T/A;C;G | snv | 1 | |||
rs11805303 | 0.827 | 0.240 | 1 | 67209833 | intron variant | C/T | snv | 0.30 | 1 | ||
rs12035082 | 1.000 | 0.040 | 1 | 172929237 | intron variant | T/C | snv | 0.52 | 1 | ||
rs12103 | 0.925 | 0.040 | 1 | 1312114 | synonymous variant | T/A;C;G | snv | 0.56 | 1 | ||
rs12567232 | 1.000 | 0.040 | 1 | 67262335 | downstream gene variant | G/A | snv | 0.27 | 1 | ||
rs1343151 | 0.752 | 0.400 | 1 | 67253446 | intron variant | G/A | snv | 0.41 | 1 | ||
rs16841904 | 0.807 | 0.160 | 1 | 197732862 | intron variant | C/T | snv | 0.18 | 1 | ||
rs17129659 | 1.000 | 0.040 | 1 | 67113712 | 3 prime UTR variant | C/A;T | snv | 8.0E-06; 6.4E-02 | 1 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 1 | ||
rs1800947 | 0.683 | 0.440 | 1 | 159713648 | splice region variant | C/A;G;T | snv | 4.4E-05; 5.1E-02; 4.0E-06 | 1 | ||
rs1998598 | 1.000 | 0.040 | 1 | 197758512 | intron variant | A/G;T | snv | 1 | |||
rs2064689 | 1.000 | 0.040 | 1 | 67187327 | intron variant | G/A | snv | 0.29 | 1 | ||
rs2488389 | 0.925 | 0.040 | 1 | 197662011 | intron variant | G/A | snv | 0.22 | 1 |