{{Rsnum
|rsid=10492096
|Gene=VAMP1
|Chromosome=12
|position=6471416
|Orientation=minus
|GMAF=0.1079
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=VAMP1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 33.6 | 61.1
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 6.8 | 93.2
| ASW | 0.0 | 12.3 | 87.7
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 4.6 | 95.4
| GIH | 9.9 | 33.7 | 56.4
| LWK | 0.0 | 15.5 | 84.5
| MEX | 1.7 | 22.4 | 75.9
| MKK | 0.0 | 5.1 | 94.9
| TSI | 2.9 | 22.5 | 74.5
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=17903296
|Trait=Hip geometry
|Title=Genome-wide association with bone mass and geometry in the Framingham Heart Study
|RiskAllele=
|Pval=0.0000030000000000000001
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10492096
|overall_frequency_n=18
|overall_frequency_d=128
|overall_frequency=0.140625
|n_genomes=12
|n_genomes_annotated=0
|n_haplomes=12
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}