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rs2396753

From SNPedia

Orientationplus
Stabilizedplus
Make rs2396753(A;A)
Make rs2396753(A;C)
Make rs2396753(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position114508276
GeneFOXP2
is asnp
is mentioned by
dbSNPrs2396753
ebirs2396753
HLIrs2396753
Exacrs2396753
Varsomers2396753
Maprs2396753
PheGenIrs2396753
hapmaprs2396753
1000 genomesrs2396753
hgdprs2396753
ensemblrs2396753
gopubmedrs2396753
geneviewrs2396753
scholarrs2396753
googlers2396753
pharmgkbrs2396753
gwascentralrs2396753
openSNPrs2396753
23andMers2396753
23andMe allrs2396753
SNP Nexus

SNPshotrs2396753
SNPdbers2396753
MSV3drs2396753
GWAS Ctlgrs2396753
GMAF0.371
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 21334420] rs2396753 (C>A) gene variant of the FOXP2 gene has significant effects on grey matter concentration in patients with schizophrenia.


[PMID 16538183] Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.


[PMID 20649982OA-icon.png] FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.


[PMID 20858950] The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.