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rs2710117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) higher risk of speech development delay and/or impairment
(A;T) None
(T;T) None
ReferenceGRCh38 38.1/141
Chromosome7
Position147904680
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs2710117
ebirs2710117
HLIrs2710117
Exacrs2710117
Varsomers2710117
Maprs2710117
PheGenIrs2710117
hapmaprs2710117
1000 genomesrs2710117
hgdprs2710117
ensemblrs2710117
gopubmedrs2710117
geneviewrs2710117
scholarrs2710117
googlers2710117
pharmgkbrs2710117
gwascentralrs2710117
openSNPrs2710117
23andMers2710117
23andMe allrs2710117
SNP Nexus

SNPshotrs2710117
SNPdbers2710117
MSV3drs2710117
GWAS Ctlgrs2710117
GMAF0.365
Max Magnitude
? (A;A) (A;T) (T;T) 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 23123147] CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population.