{{Rsnum
|rsid=8017377
|Gene=NYNRIN
|Chromosome=14
|position=24414681
|Orientation=plus
|GMAF=0.2447
|Gene_s=NYNRIN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 28.3 | 47.8 | 23.9
| HCB | 0.0 | 6.1 | 93.9
| JPT | 0.9 | 9.0 | 90.1
| YRI | 1.4 | 17.6 | 81.0
| ASW | 0.0 | 29.8 | 70.2
| CHB | 0.0 | 6.1 | 93.9
| CHD | 0.9 | 8.3 | 90.7
| GIH | 10.9 | 47.5 | 41.6
| LWK | 1.9 | 24.1 | 74.1
| MEX | 7.1 | 32.1 | 60.7
| MKK | 1.9 | 23.7 | 74.4
| TSI | 26.7 | 44.6 | 28.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=T
|Pval=4E-11
|OR=1.1700
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=NYNRIN
|aa_change=Ala978Thr
|aa_change_short=A978T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8017377
|overall_frequency_n=3765
|overall_frequency_d=10714
|overall_frequency=0.351409
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=32
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}