Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 25 | ||
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 20 | |
rs7137828 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 14 | |||
rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 12 | ||
rs6894249 | 0.776 | 0.160 | 5 | 132461855 | non coding transcript exon variant | A/G | snv | 0.45 | 9 | ||
rs2266959 | 0.776 | 0.200 | 22 | 21568615 | intron variant | G/T | snv | 0.18 | 8 | ||
rs9532434 | 0.807 | 0.120 | 13 | 39781776 | intron variant | T/A;C | snv | 8 | |||
rs2284033 | 0.790 | 0.160 | 22 | 37137994 | intron variant | G/A | snv | 0.43 | 7 | ||
rs8129030 | 0.807 | 0.120 | 21 | 35340290 | intron variant | T/A;G | snv | 0.72 | 7 | ||
rs10194635 | 0.807 | 0.120 | 2 | 100217755 | intron variant | T/A;G | snv | 6 | |||
rs10213692 | 0.807 | 0.120 | 5 | 56146422 | intron variant | T/C | snv | 0.17 | 6 | ||
rs10849448 | 0.807 | 0.120 | 12 | 6384185 | 5 prime UTR variant | A/G | snv | 0.82 | 6 | ||
rs11074967 | 0.807 | 0.120 | 16 | 11377557 | intron variant | C/G | snv | 0.36 | 6 | ||
rs11714843 | 0.807 | 0.120 | 3 | 119502217 | intron variant | T/A | snv | 0.15 | 6 | ||
rs1479924 | 0.807 | 0.120 | 4 | 122466445 | intergenic variant | G/A | snv | 0.76 | 6 | ||
rs149850873 | 0.807 | 0.120 | 18 | 12885121 | intron variant | G/A | snv | 1.7E-02 | 6 | ||
rs2476491 | 0.776 | 0.240 | 10 | 6053447 | intron variant | A/T | snv | 0.25 | 6 | ||
rs27293 | 0.807 | 0.120 | 5 | 97021474 | intron variant | A/G;T | snv | 6 | |||
rs2847293 | 0.807 | 0.120 | 18 | 12782449 | downstream gene variant | A/G;T | snv | 6 | |||
rs34132030 | 0.807 | 0.120 | 13 | 42481900 | intron variant | C/T | snv | 0.26 | 6 | ||
rs3825568 | 0.807 | 0.120 | 14 | 68793871 | 5 prime UTR variant | C/G;T | snv | 6 | |||
rs45539732 | 0.807 | 0.120 | 2 | 191009521 | intron variant | T/C | snv | 1.9E-02 | 6 | ||
rs4648881 | 0.807 | 0.120 | 1 | 24870664 | intergenic variant | G/A | snv | 0.47 | 6 | ||
rs6946509 | 0.807 | 0.120 | 7 | 22769871 | downstream gene variant | T/A;C | snv | 6 | |||
rs7069750 | 0.807 | 0.120 | 10 | 89002619 | non coding transcript exon variant | G/C;T | snv | 0.50 | 6 |