{{Rsnum
|rsid=12434716
|Gene=NPAS3
|Chromosome=14
|position=33799961
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.1322
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=NPAS3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 4.8 | 17.5 | 77.8
| HCB | 0.0 | 4.4 | 95.6
| JPT | 0.0 | 0.0 | 100.0
| YRI | 3.2 | 33.9 | 62.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 4.4 | 95.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=20466522
|Title=Association of NPAS3 exonic variation with schizophrenia
}}

{{Venter SNP
|rsid=12434716
|allele=C
|frequency=
|uid=1103649028973
|type=heterozygous_SNP
|hugo=NPAS3
|ensembl gene=ENSG00000151322
|ensembl transcript=ENST00000346562
|sift=TOLERATED
|disease=A chromosomal aberration involving NPAS3 is found in a family with schizophrenia. Translocation t(9;14)(q34;q13).
}}

{{GET Evidence
|gene=NPAS3
|aa_change=Ala539Pro
|aa_change_short=A539P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12434716
|overall_frequency_n=1820
|overall_frequency_d=10758
|overall_frequency=0.169176
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=13
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}