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rs10883866

From SNPedia

Orientationplus
Stabilizedplus
Make rs10883866(C;C)
Make rs10883866(C;G)
Make rs10883866(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position81883883
GeneNRG3
is asnp
is mentioned by
dbSNPrs10883866
dbSNP (classic)rs10883866
ClinGenrs10883866
ebirs10883866
HLIrs10883866
Exacrs10883866
Gnomadrs10883866
Varsomers10883866
LitVarrs10883866
Maprs10883866
PheGenIrs10883866
Biobankrs10883866
1000 genomesrs10883866
hgdprs10883866
ensemblrs10883866
geneviewrs10883866
scholarrs10883866
googlers10883866
pharmgkbrs10883866
gwascentralrs10883866
openSNPrs10883866
23andMers10883866
SNPshotrs10883866
SNPdbers10883866
MSV3drs10883866
GWAS Ctlgrs10883866
GMAF0.1079
Max Magnitude0
? (C;C) (C;G) (G;G) 28


rs10883866 is a SNP in the neuregulin 3 NRG3 gene.

Based on a study of 1515 Ashkenazi Jewish individuals, including 285 parent-child trios, 173 unrelated cases, and 487 unrelated controls, three SNPs (rs10883866, rs10748842, and rs6584400) were found to be associated with the "delusion" factor as a quantitative trait in schizophrenia, even though no SNP in this study withstood multiple test correction for association with the binary schizophrenia phenotype itself. After replication in an independent set of 153 Ashkenazi Jewish samples, the empirical study-wide significance across all 9 factors studied was estimated to be p = 2.7x10e-3.[PMID 19118813OA-icon.png]

OMIM608078
DescSCHIZOPHRENIA 11
Variant
Relatedalso



[PMID 20713722OA-icon.png] Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain


[PMID 20548296] Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition.



[PMID 28256518OA-icon.png] Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.