Source: GWASDB ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10478730 | 6 | 12297276 | downstream gene variant | C/T | snv | 1.2E-02 | 5 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 4 | ||||
rs11076175 | 16 | 56972466 | intron variant | A/G | snv | 0.20 | 5 | ||||
rs11076176 | 16 | 56973534 | intron variant | T/A;G | snv | 2.4E-05; 0.22 | 4 | ||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 5 | ||||
rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
rs11571111 | 1 | 204161105 | intron variant | C/A | snv | 5.0E-03 | 4 | ||||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs11635491 | 15 | 58427542 | intron variant | G/A | snv | 0.27 | 4 | ||||
rs11873890 | 18 | 662135 | intron variant | A/G | snv | 8.2E-03 | 3.2E-02 | 4 | |||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
rs11960617 | 5 | 156494033 | intron variant | C/T | snv | 1.9E-02 | 3 | ||||
rs11999657 | 9 | 21078937 | upstream gene variant | G/A;C | snv | 3 | |||||
rs12097137 | 1 | 101243889 | downstream gene variant | G/A;T | snv | 3 | |||||
rs12242772 | 10 | 87944637 | intron variant | A/G | snv | 3.0E-02 | 3 | ||||
rs12247406 | 10 | 106996746 | intron variant | G/A | snv | 1.3E-02 | 3 | ||||
rs12285095 | 11 | 116787315 | non coding transcript exon variant | T/G | snv | 9.8E-02 | 4 | ||||
rs12287066 | 11 | 116791615 | synonymous variant | G/T | snv | 7.7E-02 | 0.10 | 4 | |||
rs12341993 | 9 | 104896629 | intron variant | C/A;T | snv | 3 | |||||
rs12720922 | 16 | 56966973 | intron variant | G/A | snv | 0.23 | 4 | ||||
rs12721046 | 19 | 44917997 | intron variant | G/A | snv | 0.11 | 8 | ||||
rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
rs13284054 | 9 | 104906792 | intron variant | T/C | snv | 0.12 | 3 | ||||
rs13290420 | 9 | 104886684 | intron variant | T/C | snv | 0.16 | 3 |