Source: GWASDB ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10107815 | 8 | 10156645 | intron variant | G/C | snv | 5.1E-02 | 4 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs10271556 | 7 | 106258428 | intron variant | C/T | snv | 5.6E-02 | 4 | ||||
rs10402729 | 19 | 19244291 | intron variant | T/C | snv | 3.3E-02 | 4 | ||||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 7 | |
rs10478730 | 6 | 12297276 | downstream gene variant | C/T | snv | 1.2E-02 | 5 | ||||
rs10484766 | 6 | 131578846 | intron variant | C/T | snv | 3.3E-02 | 4 | ||||
rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
rs11568767 | 9 | 99132990 | intron variant | C/T | snv | 3.7E-03 | 4 | ||||
rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 6 | |||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs11574980 | 13 | 46105177 | non coding transcript exon variant | T/C | snv | 2.1E-02 | 4 | ||||
rs11828157 | 11 | 102947395 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
rs12394306 | X | 47576648 | splice region variant | A/C;T | snv | 4.3E-03 | 4 | ||||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 5 | ||
rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 10 | ||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 11 | ||
rs16830551 | 3 | 119834031 | intron variant | C/T | snv | 2.4E-02 | 4 | ||||
rs16860926 | 3 | 186609982 | intron variant | T/C | snv | 2.6E-02 | 4 |