Rs761100

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is asnp
is mentioned by
dbSNPrs761100
hapmaprs761100
hgdprs761100
ensemblrs761100
gopubmedrs761100
scholarrs761100
googlers761100
pharmgkbrs761100
hgvbaseg2prs761100
medrefsnprs761100
23andMers761100
SNP Nexus

GeneKIAA0319
Chromosome6
Orientationminus
Position24740620
GenotypeEffect
rs761100(G;G)higher risk for dyslexia
rs761100(G;T)normal risk
rs761100(T;T)normal risk


Genotypes Magnitude Summary
Rs761100(A;A) 00
Rs761100(A;C) 00
Rs761100(G;G) higher risk for dyslexia
Rs761100(G;T) normal risk
Rs761100(T;T) normal risk
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]
? (G;G) (G;T) (T;T)
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