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rs9467076

From SNPedia

Orientationplus
Stabilizedplus
Make rs9467076(C;C)
Make rs9467076(C;T)
Make rs9467076(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position24209027
GeneDCDC2
is asnp
is mentioned by
dbSNPrs9467076
ebirs9467076
HLIrs9467076
Exacrs9467076
Varsomers9467076
Maprs9467076
PheGenIrs9467076
hapmaprs9467076
1000 genomesrs9467076
hgdprs9467076
ensemblrs9467076
gopubmedrs9467076
geneviewrs9467076
scholarrs9467076
googlers9467076
pharmgkbrs9467076
gwascentralrs9467076
openSNPrs9467076
23andMers9467076
23andMe allrs9467076
SNP Nexus

SNPshotrs9467076
SNPdbers9467076
MSV3drs9467076
GWAS Ctlgrs9467076
GMAF0.09229
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20068590OA-icon.png] Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
OMIM600202
Desc
Variant
Relatedalso
[PMID 16385449OA-icon.png] Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.