rs2075799
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2075799(A;A) |
| Make rs2075799(A;G) |
| Make rs2075799(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31810752 |
| Gene | HSPA1L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075799 |
| dbSNP (classic) | rs2075799 |
| ClinGen | rs2075799 |
| ebi | rs2075799 |
| HLI | rs2075799 |
| Exac | rs2075799 |
| Gnomad | rs2075799 |
| Varsome | rs2075799 |
| LitVar | rs2075799 |
| Map | rs2075799 |
| PheGenI | rs2075799 |
| Biobank | rs2075799 |
| 1000 genomes | rs2075799 |
| hgdp | rs2075799 |
| ensembl | rs2075799 |
| geneview | rs2075799 |
| scholar | rs2075799 |
| rs2075799 | |
| pharmgkb | rs2075799 |
| gwascentral | rs2075799 |
| openSNP | rs2075799 |
| 23andMe | rs2075799 |
| SNPshot | rs2075799 |
| SNPdbe | rs2075799 |
| MSV3d | rs2075799 |
| GWAS Ctlg | rs2075799 |
| GMAF | 0.1428 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19766166] TAAR 6 and HSP-70 variations associated with bipolar disorder
[PMID 18299791] Association analysis of heat shock protein 70 gene polymorphisms in schizophrenia.
[PMID 19439993] The impact of heat shock protein 70 gene variations on clinical presentation and outcome in schizophrenic inpatients.
| GWAS snp | |
|---|---|
| PMID | [PMID 23028341 ]
|
| Trait | Complement C3 and C4 levels |
| Title | Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. |
| Risk Allele | T |
| P-val | 6E-97 |
| Odds Ratio | .17 [0.15-0.19] g/L decrease |
