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rs9722

From SNPedia

Orientationminus
Stabilizedminus
Make rs9722(C;C)
Make rs9722(C;T)
Make rs9722(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position46599326
GeneS100B
is asnp
is mentioned by
dbSNPrs9722
ebirs9722
HLIrs9722
Exacrs9722
Varsomers9722
Maprs9722
PheGenIrs9722
hapmaprs9722
1000 genomesrs9722
hgdprs9722
ensemblrs9722
gopubmedrs9722
geneviewrs9722
scholarrs9722
googlers9722
pharmgkbrs9722
gwascentralrs9722
openSNPrs9722
23andMers9722
23andMe allrs9722
SNP Nexus

SNPshotrs9722
SNPdbers9722
MSV3drs9722
GWAS Ctlgrs9722
GMAF0.2557
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19497163] Association study of astrocyte-derived protein S100B gene polymorphisms with major depressive disorder in Chinese people.

[PMID 21070816] Risk variants in the S100B gene, associated with elevated S100B levels, are also associated with visuospatial disability of schizophrenia.

[PMID 22019077] S100B gene polymorphisms predict prefrontal spatial function in both schizophrenia patients and healthy individuals.

[PMID 15670788] SNPs and haplotypes in the S100B gene reveal association with schizophrenia.

[PMID 18939940] No association of the rs9722 C >T in the S100B gene and susceptibility to major depression in a Chinese population.

[PMID 19330775] Risk variants in the S100B gene predict elevated S100B serum concentrations in healthy individuals.

[PMID 20559426OA-icon.png] Serum S100B: a potential biomarker for suicidality in adolescents?