{{Rsnum
|rsid=2236316
|Gene=NIN
|Chromosome=14
|position=50757699
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|GMAF=0.1841
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=NIN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 10.8 | 43.1 | 46.2
| HCB | 2.2 | 26.7 | 71.1
| JPT | 4.5 | 27.3 | 68.2
| YRI | 0.0 | 9.5 | 90.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 26.7 | 71.1
| 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
}}{{Venter SNP
|rsid=2236316
|allele=C
|frequency=0.325
|uid=1103649060175
|type=heterozygous_SNP
|hugo=NIN
|ensembl gene=ENSG00000100503
|ensembl transcript=ENST00000382041
|sift=TOLERATED
|disease=Antibodies against NIN are present in sera from patients with autoimmune diseases that developed autoantibodies against centrosomal proteins.
}}

{{ neighbor
| rsid = 2073347
| distance = 628
}}

{{GET Evidence
|gene=NIN
|aa_change=Pro1111Ala
|aa_change_short=P1111A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2236316
|overall_frequency_n=2140
|overall_frequency_d=10758
|overall_frequency=0.198922
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.003
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}