{{Rsnum
|rsid=2073347
|Gene=NIN
|Chromosome=14
|position=50757071
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.2314
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NIN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 32.7 | 59.3
| HCB | 16.2 | 39.0 | 44.9
| JPT | 8.0 | 30.1 | 61.9
| YRI | 1.4 | 19.0 | 79.6
| ASW | 7.0 | 35.1 | 57.9
| CHB | 16.2 | 39.0 | 44.9
| CHD | 7.3 | 42.2 | 50.5
| GIH | 9.1 | 47.5 | 43.4
| LWK | 0.9 | 21.8 | 77.3
| MEX | 1.7 | 31.0 | 67.2
| MKK | 9.0 | 30.3 | 60.6
| TSI | 5.9 | 31.4 | 62.7
| HapMapRevision=28
}}

{{Venter SNP
|rsid=2073347
|allele=T
|frequency=0.792
|uid=1103649060186
|type=homozygous_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 = 2236316
| distance = 628
}}

{{GET Evidence
|gene=NIN
|aa_change=Gly1320Glu
|aa_change_short=G1320E
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2073347
|overall_frequency_n=8524
|overall_frequency_d=10758
|overall_frequency=0.792341
|n_genomes=54
|n_genomes_annotated=0
|n_haplomes=95
|n_articles=0
|n_articles_annotated=0
|nblosum100=6
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}