{{Rsnum
|rsid=11544636
|Gene=NRSN1
|Chromosome=6
|position=24145668
|Orientation=plus
|GMAF=0.008264
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NRSN1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 93.8 | 6.2 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 88.0 | 12.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 98.2 | 1.8 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 94.1 | 5.9 | 0.0
| HapMapRevision=28
}}

{{PMID Auto
|PMID=16385449
|Title=Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
|OA=1
}}

{{GET Evidence
|gene=NRSN1
|aa_change=His104Tyr
|aa_change_short=H104Y
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11544636
|overall_frequency_n=179
|overall_frequency_d=10758
|overall_frequency=0.0166388
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.899
|nblosum100=-1
|autoscore=2
|webscore=N
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}