{{Rsnum
|rsid=2272996
|Gene=VNN1
|Chromosome=6
|position=132694132
|Orientation=plus
|GMAF=0.2736
|Gene_s=VNN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 39.8 | 50.4
| HCB | 18.2 | 46.0 | 35.8
| JPT | 18.6 | 49.6 | 31.9
| YRI | 4.1 | 29.3 | 66.7
| ASW | 1.8 | 31.6 | 66.7
| CHB | 18.2 | 46.0 | 35.8
| CHD | 14.8 | 45.4 | 39.8
| GIH | 8.9 | 35.6 | 55.4
| LWK | 0.9 | 31.8 | 67.3
| MEX | 1.7 | 31.0 | 67.2
| MKK | 5.2 | 24.8 | 69.9
| TSI | 7.8 | 38.2 | 53.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=18043751
|Title=Admixture Mapping Provides Evidence of Association of the VNN1 Gene with Hypertension
|OA=1
}}

{{GET Evidence
|gene=VNN1
|aa_change=Asn131Ser
|aa_change_short=N131S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2272996
|overall_frequency_n=2596
|overall_frequency_d=10758
|overall_frequency=0.241309
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=36
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.996
|nblosum100=0
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=25233454
|Title=The Association of the Vanin-1 N131S Variant with Blood Pressure Is Mediated by Endoplasmic Reticulum-Associated Degradation and Loss of Function
}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}