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rs4234898

From SNPedia

Orientationplus
Stabilizedplus
Make rs4234898(C;C)
Make rs4234898(C;T)
Make rs4234898(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position156077389
is asnp
is mentioned by
dbSNPrs4234898
ebirs4234898
HLIrs4234898
Exacrs4234898
Varsomers4234898
Maprs4234898
PheGenIrs4234898
hapmaprs4234898
1000 genomesrs4234898
hgdprs4234898
ensemblrs4234898
gopubmedrs4234898
geneviewrs4234898
scholarrs4234898
googlers4234898
pharmgkbrs4234898
gwascentralrs4234898
openSNPrs4234898
23andMers4234898
23andMe allrs4234898
SNP Nexus

SNPshotrs4234898
SNPdbers4234898
MSV3drs4234898
GWAS Ctlgrs4234898
GMAF0.1331
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19786962]
Trait Speech perception in dyslexia
Title First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
Risk Allele T
P-val 5E-8
Odds Ratio NR NR


GET Evidence
rs4234898
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.804688
summary