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rs1007371

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 1.2 rare genotype.
Make rs1007371(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position80326220
GeneCTNNA2
is asnp
is mentioned by
dbSNPrs1007371
ebirs1007371
HLIrs1007371
Exacrs1007371
Varsomers1007371
Maprs1007371
PheGenIrs1007371
hapmaprs1007371
1000 genomesrs1007371
hgdprs1007371
ensemblrs1007371
gopubmedrs1007371
geneviewrs1007371
scholarrs1007371
googlers1007371
pharmgkbrs1007371
gwascentralrs1007371
openSNPrs1007371
23andMers1007371
23andMe allrs1007371
SNP Nexus

SNPshotrs1007371
SNPdbers1007371
MSV3drs1007371
GWAS Ctlgrs1007371
GMAF0.2052
Max Magnitude1.2
[PMID 17667961OA-icon.png] having minor alleles at all 3 of rs1446109-rs1007371-rs723524 may affect left-right asymmetrical brain function, such as handedness, and much of human cognition, behavior and emotion. pdf full paper