Rs761100

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Orientationminus
Geno Mag Summary
(G;G) higher risk for dyslexia
(G;T) 0 normal risk
(T;T) 0 normal risk
ReferenceGRCh38 38.1/141
Chromosome6
Position24632414
GeneKIAA0319
is asnp
is mentioned by
dbSNPrs761100
Exacrs761100
PheGenIrs761100
nextbiors761100
hapmaprs761100
1000 genomesrs761100
hgdprs761100
ensemblrs761100
gopubmedrs761100
geneviewrs761100
scholarrs761100
googlers761100
pharmgkbrs761100
gwascentralrs761100
openSNPrs761100
23andMers761100
23andMe allrs761100
SNP Nexus

SNPshotrs761100
SNPdbers761100
MSV3drs761100
GMAF0.3173
Max Magnitude0
? (G;G) (G;T) (T;T) 28
The more common allele of rs761100 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 19997522OA-icon.png] Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.

Developmental Dyslexia