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rs11544636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11544636(C;T)
Make rs11544636(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position24145668
GeneNRSN1
is asnp
is mentioned by
dbSNPrs11544636
ebirs11544636
HLIrs11544636
Exacrs11544636
Varsomers11544636
Maprs11544636
PheGenIrs11544636
hapmaprs11544636
1000 genomesrs11544636
hgdprs11544636
ensemblrs11544636
gopubmedrs11544636
geneviewrs11544636
scholarrs11544636
googlers11544636
pharmgkbrs11544636
gwascentralrs11544636
openSNPrs11544636
23andMers11544636
23andMe allrs11544636
SNP Nexus

SNPshotrs11544636
SNPdbers11544636
MSV3drs11544636
GWAS Ctlgrs11544636
GMAF0.008264
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 16385449OA-icon.png] Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.


GET Evidence
NRSN1-H104Y
aa_change His104Tyr
aa_change_short H104Y
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0166388
summary