{{Rsnum
|rsid=222747
|Gene=TRPV1
|Chromosome=17
|position=3589906
|Orientation=minus
|GMAF=0.3007
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=TRPV1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 66.2 | 30.8 | 3.1
| HCB | 17.8 | 55.6 | 26.7
| JPT | 15.9 | 54.5 | 29.5
| YRI | 88.9 | 11.1 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 17.8 | 55.6 | 26.7
| 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
}}{{PMID Auto
|PMID=20034385
|Title=Polymorphisms in gene encoding TRPV1-receptor involved in pain perception are unrelated to chronic pancreatitis
|OA=1
}}

{{PMID|18520591|OA=1
}} Sequence variants in host cell factor C1 are associated with Meniere's disease.

{{GET Evidence
|gene=TRPV1
|aa_change=Met315Ile
|aa_change_short=M315I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs222747
|overall_frequency_n=8430
|overall_frequency_d=10492
|overall_frequency=0.803469
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=92
|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 | HumanOmni1Quad}}