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rs479526

From SNPedia

Orientationplus
Stabilizedplus
Make rs479526(C;C)
Make rs479526(C;T)
Make rs479526(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position11617934
is asnp
is mentioned by
dbSNPrs479526
ebirs479526
HLIrs479526
Exacrs479526
Varsomers479526
Maprs479526
PheGenIrs479526
hapmaprs479526
1000 genomesrs479526
hgdprs479526
ensemblrs479526
gopubmedrs479526
geneviewrs479526
scholarrs479526
googlers479526
pharmgkbrs479526
gwascentralrs479526
openSNPrs479526
23andMers479526
23andMe allrs479526
SNP Nexus

SNPshotrs479526
SNPdbers479526
MSV3drs479526
GWAS Ctlgrs479526
GMAF0.4821
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23738518OA-icon.png]
Trait Reading and spelling
Title A genome-wide association study for reading and language abilities in two population cohorts.
Risk Allele T
P-val 3E-6
Odds Ratio .09 [0.054-0.132]