{{Rsnum
|rsid=4234898
|Chromosome=4
|position=156077389
|Orientation=plus
|GMAF=0.1331
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 75.0 | 24.1 | 0.9
| HCB | 70.8 | 28.5 | 0.7
| JPT | 79.6 | 20.4 | 0.0
| YRI | 55.8 | 38.8 | 5.4
| ASW | 71.9 | 22.8 | 5.3
| CHB | 70.8 | 28.5 | 0.7
| CHD | 78.9 | 19.3 | 1.8
| GIH | 66.3 | 27.7 | 5.9
| LWK | 68.8 | 28.4 | 2.8
| MEX | 71.9 | 28.1 | 0.0
| MKK | 71.8 | 25.0 | 3.2
| TSI | 83.3 | 15.7 | 1.0
| 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=T
|Pval=5E-8
|OR=NR
|ORtxt=NR
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4234898
|overall_frequency_n=103
|overall_frequency_d=128
|overall_frequency=0.804688
|n_genomes=54
|n_genomes_annotated=0
|n_haplomes=94
|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 | Illumina Human 1M}}