Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11111 | 0.882 | 0.080 | 5 | 37814000 | 3 prime UTR variant | T/C | snv | 0.22 | 5 | ||
rs13440581 | 0.882 | 0.080 | X | 151181399 | missense variant | A/G | snv | 0.45 | 0.45 | 5 | |
rs2070587 | 0.882 | 0.080 | 12 | 108883967 | intron variant | T/G | snv | 0.32 | 5 | ||
rs2072115 | 0.882 | 0.080 | 12 | 47751585 | intron variant | A/C;G | snv | 5 | |||
rs228697 | 0.882 | 0.080 | 1 | 7827519 | missense variant | C/G | snv | 8.7E-02 | 7.3E-02 | 5 | |
rs3096140 | 0.882 | 0.080 | 5 | 37832731 | intron variant | G/A | snv | 0.69 | 5 | ||
rs2349775 | 0.851 | 0.120 | 7 | 8678450 | intron variant | G/A;C | snv | 6 | |||
rs41305272 | 0.851 | 0.120 | 15 | 67807105 | 3 prime UTR variant | C/T | snv | 2.4E-02 | 6 | ||
rs1202184 | 0.851 | 0.120 | 7 | 87584585 | intron variant | C/T | snv | 0.39 | 7 | ||
rs2072621 | 0.851 | 0.080 | X | 151177387 | non coding transcript exon variant | C/A;G | snv | 7 | |||
rs2740210 | 0.827 | 0.120 | 20 | 3072609 | downstream gene variant | C/A | snv | 0.28 | 7 | ||
rs57875989 | 0.882 | 0.080 | 1 | 7829913 | splice acceptor variant | GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC | delins | 0.11 | 0.18 | 7 | |
rs7194256 | 0.827 | 0.120 | 16 | 55703779 | 3 prime UTR variant | C/G;T | snv | 7 | |||
rs7766029 | 0.851 | 0.080 | 6 | 88137716 | downstream gene variant | T/C | snv | 0.51 | 7 | ||
rs1922242 | 0.827 | 0.120 | 7 | 87544351 | intron variant | A/T | snv | 0.43 | 8 | ||
rs900418273 | 0.807 | 0.120 | 11 | 113393764 | missense variant | A/G | snv | 8 | |||
rs1881457 | 0.790 | 0.280 | 5 | 132656717 | intron variant | A/C | snv | 0.21 | 9 | ||
rs2020936 | 0.776 | 0.160 | 17 | 30223796 | intron variant | G/A;C | snv | 10 | |||
rs2298383 | 0.827 | 0.200 | 22 | 24429543 | non coding transcript exon variant | C/A;T | snv | 11 | |||
rs3213207 | 0.776 | 0.120 | 6 | 15627871 | intron variant | T/C | snv | 8.7E-02 | 11 | ||
rs4713916 | 0.790 | 0.160 | 6 | 35702206 | intron variant | A/C;G;T | snv | 11 | |||
rs9470080 | 0.827 | 0.080 | 6 | 35678658 | intron variant | T/A;C | snv | 13 | |||
rs3219151 | 0.752 | 0.160 | 5 | 161701908 | 3 prime UTR variant | C/T | snv | 0.51 | 14 | ||
rs6354 | 0.732 | 0.280 | 17 | 30222880 | 5 prime UTR variant | G/C;T | snv | 16 | |||
rs9296158 | 0.763 | 0.080 | 6 | 35599305 | intron variant | A/G | snv | 0.65 | 16 |