Have questions? Visit https://www.reddit.com/r/SNPedia

rs3212236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) higher risk for dyslexia
(A;G) normal risk
(C;T) 0
(G;G) normal risk
ReferenceGRCh38 38.1/141
Chromosome6
Position24648227
GeneTTRAP
is asnp
is mentioned by
dbSNPrs3212236
dbSNP (classic)rs3212236
ClinGenrs3212236
ebirs3212236
HLIrs3212236
Exacrs3212236
Gnomadrs3212236
Varsomers3212236
LitVarrs3212236
Maprs3212236
PheGenIrs3212236
Biobankrs3212236
1000 genomesrs3212236
hgdprs3212236
ensemblrs3212236
geneviewrs3212236
scholarrs3212236
googlers3212236
pharmgkbrs3212236
gwascentralrs3212236
openSNPrs3212236
23andMers3212236
SNPshotrs3212236
SNPdbers3212236
MSV3drs3212236
GWAS Ctlgrs3212236
GMAF0.3287
Max Magnitude0

The more common allele of rs3212236 has been linked to increased risk for developmental dyslexia in a study of ~300 British families. While odds ratios were not reported, the significance was reported as p=0.02.[PMID 17033633]


[PMID 15717286OA-icon.png] Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.


[PMID 19325871OA-icon.png] A common variant associated with dyslexia reduces expression of the KIAA0319 gene.