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rs1922892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) None
(C;T) None
(T;T) higher risk of speech development delay and/or impairment
ReferenceGRCh38 38.1/141
Chromosome7
Position147879319
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1922892
ebirs1922892
HLIrs1922892
Exacrs1922892
Varsomers1922892
Maprs1922892
PheGenIrs1922892
hapmaprs1922892
1000 genomesrs1922892
hgdprs1922892
ensemblrs1922892
gopubmedrs1922892
geneviewrs1922892
scholarrs1922892
googlers1922892
pharmgkbrs1922892
gwascentralrs1922892
openSNPrs1922892
23andMers1922892
23andMe allrs1922892
SNP Nexus

SNPshotrs1922892
SNPdbers1922892
MSV3drs1922892
GWAS Ctlgrs1922892
GMAF0.4008
Max Magnitude
Reported to be in very tight (r2>0.98) linkage with rs2710102, and thus potentially associated with autism.

[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 18179893OA-icon.png] Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.