rs79681911
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs79681911(A;A) |
| Make rs79681911(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 18269755 |
| Gene | SAA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79681911 |
| dbSNP (classic) | rs79681911 |
| ClinGen | rs79681911 |
| ebi | rs79681911 |
| HLI | rs79681911 |
| Exac | rs79681911 |
| Gnomad | rs79681911 |
| Varsome | rs79681911 |
| LitVar | rs79681911 |
| Map | rs79681911 |
| PheGenI | rs79681911 |
| Biobank | rs79681911 |
| 1000 genomes | rs79681911 |
| hgdp | rs79681911 |
| ensembl | rs79681911 |
| geneview | rs79681911 |
| scholar | rs79681911 |
| rs79681911 | |
| pharmgkb | rs79681911 |
| gwascentral | rs79681911 |
| openSNP | rs79681911 |
| 23andMe | rs79681911 |
| SNPshot | rs79681911 |
| SNPdbe | rs79681911 |
| MSV3d | rs79681911 |
| GWAS Ctlg | rs79681911 |
| GMAF | 0.006887 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79681911(A;A) |
| Alt | rs79681911(A;A) |
| Reference | Rs79681911(G;G) |
| Significance | Pathogenic |
| Disease | Serum amyloid a variant |
| Variation | info |
| Gene | SAA1 |
| CLNDBN | Serum amyloid a variant |
| Reversed | 0 |
| HGVS | NC_000011.9:g.18291302G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019735.27, |
