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 |