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rs13227425

From SNPedia

Orientationplus
Stabilizedplus
Make rs13227425(C;C)
Make rs13227425(C;T)
Make rs13227425(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position13514383
is asnp
is mentioned by
dbSNPrs13227425
ebirs13227425
HLIrs13227425
Exacrs13227425
Varsomers13227425
Maprs13227425
PheGenIrs13227425
hapmaprs13227425
1000 genomesrs13227425
hgdprs13227425
ensemblrs13227425
gopubmedrs13227425
geneviewrs13227425
scholarrs13227425
googlers13227425
pharmgkbrs13227425
gwascentralrs13227425
openSNPrs13227425
23andMers13227425
23andMe allrs13227425
SNP Nexus

SNPshotrs13227425
SNPdbers13227425
MSV3drs13227425
GWAS Ctlgrs13227425
GMAF0.1419
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23738518OA-icon.png]
Trait Word reading
Title A genome-wide association study for reading and language abilities in two population cohorts.
Risk Allele
P-val 7E-6
Odds Ratio NR NR