{{Rsnum
|rsid=4751178
|Chromosome=10
|position=131992245
|Orientation=plus
|GMAF=0.2769
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 8.0 | 46.0 | 46.0
| HCB | 16.1 | 50.4 | 33.6
| JPT | 6.2 | 39.8 | 54.0
| YRI | 5.4 | 31.3 | 63.3
| ASW | 5.3 | 28.1 | 66.7
| CHB | 16.1 | 50.4 | 33.6
| CHD | 9.2 | 54.1 | 36.7
| GIH | 10.9 | 33.7 | 55.4
| LWK | 3.6 | 28.2 | 68.2
| MEX | 5.2 | 37.9 | 56.9
| MKK | 5.1 | 35.3 | 59.6
| TSI | 10.8 | 35.3 | 53.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|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
|RiskAllele=G
|Pval=0.000007
|OR=NR
|ORtxt=NR
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4751178
|overall_frequency_n=85
|overall_frequency_d=120
|overall_frequency=0.708333
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=71
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}