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rs4751178

From SNPedia

Orientationplus
Stabilizedplus
Make rs4751178(A;A)
Make rs4751178(A;G)
Make rs4751178(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position130193981
is asnp
is mentioned by
dbSNPrs4751178
ebirs4751178
HLIrs4751178
Exacrs4751178
Varsomers4751178
Maprs4751178
PheGenIrs4751178
hapmaprs4751178
1000 genomesrs4751178
hgdprs4751178
ensemblrs4751178
gopubmedrs4751178
geneviewrs4751178
scholarrs4751178
googlers4751178
pharmgkbrs4751178
gwascentralrs4751178
openSNPrs4751178
23andMers4751178
23andMe allrs4751178
SNP Nexus

SNPshotrs4751178
SNPdbers4751178
MSV3drs4751178
GWAS Ctlgrs4751178
GMAF0.2769
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000007
Odds Ratio NR NR


GET Evidence
rs4751178
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.708333
summary