Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75634836 | 0.807 | 0.160 | 13 | 46835532 | missense variant | C/A;T | snv | 4.0E-06 | 11 | ||
rs2271933 | 0.807 | 0.080 | 1 | 31626924 | missense variant | A/G | snv | 0.56 | 0.50 | 9 | |
rs3813034 | 0.827 | 0.160 | 17 | 30197786 | 3 prime UTR variant | A/C | snv | 0.40 | 8 | ||
rs4565946 | 0.827 | 0.080 | 12 | 71942989 | intron variant | C/A;G;T | snv | 7 | |||
rs3749034 | 0.827 | 0.040 | 2 | 170816965 | 5 prime UTR variant | G/A;T | snv | 6 | |||
rs17689918 | 0.851 | 0.080 | 17 | 45832722 | intron variant | G/A | snv | 0.15 | 6 | ||
rs1173546708 | 0.851 | 0.120 | 11 | 18040661 | synonymous variant | G/A | snv | 4.0E-06 | 5 | ||
rs1245554802 | 0.851 | 0.120 | 3 | 9765892 | splice acceptor variant | T/C | snv | 4.0E-06 | 5 | ||
rs4722999 | 0.851 | 0.080 | 7 | 30654159 | intron variant | C/T | snv | 0.67 | 5 | ||
rs771306418 | 0.851 | 0.120 | 3 | 9765885 | splice acceptor variant | -/C | delins | 5 | |||
rs1800857 | 0.851 | 0.120 | 4 | 26489489 | splice region variant | A/G | snv | 0.17 | 0.18 | 4 | |
rs945032 | 0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 | 5 | ||
rs12579350 | 0.882 | 0.080 | 12 | 5687935 | intron variant | G/A | snv | 0.12 | 3 | ||
rs173365 | 0.882 | 0.080 | 17 | 45823708 | intron variant | A/G | snv | 0.55 | 3 | ||
rs242924 | 0.882 | 0.080 | 17 | 45808001 | intron variant | G/T | snv | 0.44 | 3 | ||
rs17466684 | 0.925 | 0.120 | 8 | 27595330 | downstream gene variant | G/A | snv | 0.15 | 5 | ||
rs2296972 | 0.925 | 0.080 | 13 | 46854336 | intron variant | A/C | snv | 0.70 | 4 | ||
rs10801153 | 0.925 | 0.080 | 1 | 192794818 | intron variant | G/A | snv | 0.27 | 3 | ||
rs2910931 | 0.925 | 0.080 | 5 | 32394809 | intron variant | T/A | snv | 0.63 | 3 | ||
rs10216809 | 0.925 | 0.080 | 8 | 14507414 | intron variant | C/G;T | snv | 2 | |||
rs10894993 | 0.925 | 0.080 | 11 | 100627998 | intergenic variant | T/G | snv | 4.7E-02 | 2 | ||
rs11179000 | 0.925 | 0.040 | 12 | 71944848 | intron variant | A/T | snv | 0.31 | 2 | ||
rs11210604 | 0.925 | 0.080 | 1 | 42158001 | downstream gene variant | T/A;G | snv | 2 | |||
rs11724320 | 0.925 | 0.040 | 4 | 163346771 | intron variant | T/C | snv | 0.56 | 2 | ||
rs11946004 | 0.925 | 0.040 | 4 | 163351551 | synonymous variant | G/A;T | snv | 0.10; 4.0E-06 | 2 |