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rs2538976

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) None
(A;G) None
(G;G) higher risk for speech development delay and/or impairment
ReferenceGRCh38 38.1/141
Chromosome7
Position147888727
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs2538976
ebirs2538976
HLIrs2538976
Exacrs2538976
Varsomers2538976
Maprs2538976
PheGenIrs2538976
hapmaprs2538976
1000 genomesrs2538976
hgdprs2538976
ensemblrs2538976
gopubmedrs2538976
geneviewrs2538976
scholarrs2538976
googlers2538976
pharmgkbrs2538976
gwascentralrs2538976
openSNPrs2538976
23andMers2538976
23andMe allrs2538976
SNP Nexus

SNPshotrs2538976
SNPdbers2538976
MSV3drs2538976
GWAS Ctlgrs2538976
GMAF0.4692
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18987363OA-icon.png] Speech development rs4431523, rs17236239 and significant associations (with P values from 0.01 to 5.0x10–5) between nonsense-word repetition and nine intronic SNPs (rs851715, rs10246256, rs2710102, rs759178, rs1922892, rs2538991, rs17236239, rs2538976, and rs2710117)


[PMID 21310003OA-icon.png] CNTNAP2 variants affect early language development in the general population.