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rs362719

From SNPedia

Orientationplus
Stabilizedplus
Make rs362719(A;A)
Make rs362719(A;C)
Make rs362719(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position103545430
GeneRELN
is asnp
is mentioned by
dbSNPrs362719
ebirs362719
HLIrs362719
Exacrs362719
Varsomers362719
Maprs362719
PheGenIrs362719
hapmaprs362719
1000 genomesrs362719
hgdprs362719
ensemblrs362719
gopubmedrs362719
geneviewrs362719
scholarrs362719
googlers362719
pharmgkbrs362719
gwascentralrs362719
openSNPrs362719
23andMers362719
23andMe allrs362719
SNP Nexus

SNPshotrs362719
SNPdbers362719
MSV3drs362719
GWAS Ctlgrs362719
GMAF0.3439
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 21863557] A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han


[PMID 18597938] Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.


[PMID 19691043OA-icon.png] Sex-specific association of the Reelin gene with bipolar disorder.