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rs2075799

From SNPedia

Orientationminus
Stabilizedminus
Make rs2075799(A;A)
Make rs2075799(A;G)
Make rs2075799(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31810752
GeneHSPA1L
is asnp
is mentioned by
dbSNPrs2075799
ebirs2075799
HLIrs2075799
Exacrs2075799
Varsomers2075799
Maprs2075799
PheGenIrs2075799
hapmaprs2075799
1000 genomesrs2075799
hgdprs2075799
ensemblrs2075799
gopubmedrs2075799
geneviewrs2075799
scholarrs2075799
googlers2075799
pharmgkbrs2075799
gwascentralrs2075799
openSNPrs2075799
23andMers2075799
23andMe allrs2075799
SNP Nexus

SNPshotrs2075799
SNPdbers2075799
MSV3drs2075799
GWAS Ctlgrs2075799
GMAF0.1428
Max Magnitude
? (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 23028341OA-icon.png]
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