rs634552
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | Normal |
| (T;T) | 1 | AMD Association |
| Make rs634552(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 75571007 |
| Gene | SERPINH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs634552 |
| dbSNP (classic) | rs634552 |
| ClinGen | rs634552 |
| ebi | rs634552 |
| HLI | rs634552 |
| Exac | rs634552 |
| Gnomad | rs634552 |
| Varsome | rs634552 |
| LitVar | rs634552 |
| Map | rs634552 |
| PheGenI | rs634552 |
| Biobank | rs634552 |
| 1000 genomes | rs634552 |
| hgdp | rs634552 |
| ensembl | rs634552 |
| geneview | rs634552 |
| scholar | rs634552 |
| rs634552 | |
| pharmgkb | rs634552 |
| gwascentral | rs634552 |
| openSNP | rs634552 |
| 23andMe | rs634552 |
| SNPshot | rs634552 |
| SNPdbe | rs634552 |
| MSV3d | rs634552 |
| GWAS Ctlg | rs634552 |
| GMAF | 0.3145 |
| Max Magnitude | 1 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height |
| Risk Allele | T |
| P-val | 4E-13 |
| Odds Ratio | 0.04 [NR] unit increase |
Single variant analysis of variants significantly associated with AMD risk
[PMID 28347358] Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.
