{{Rsnum
|rsid=3742030
|Gene=TRPV4
|Chromosome=12
|position=109814742
|Orientation=minus
|GMAF=0.04454
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TRPV4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 98.5 | 1.5 | 0.0
| HCB | 95.2 | 4.8 | 0.0
| JPT | 88.4 | 11.6 | 0.0
| YRI | 90.5 | 9.5 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 95.2 | 4.8 | 0.0
| 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
}}{{omim
|id=605427
|desc=TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY V, MEMBER 4;
|rsnum=3742030
}}

{{omim
|id=605427
|rsnum=3742030
|variant=0012
}}

{{GET Evidence
|gene=TRPV4
|aa_change=Pro19Ser
|aa_change_short=P19S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3742030
|overall_frequency_n=321
|overall_frequency_d=10692
|overall_frequency=0.0300224
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.001
|genetests_testable=Y
|nblosum100=3
|autoscore=2
|n_web_uneval=6
}}
{{ClinVar
|ALT=A
|CAF=0.9555; 0.04454
|CHROM=12
|CLNACC=RCV000005297.1
|CLNALLE=1
|CLNDBN=Sodium serum level quantitative trait locus 1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3150755:613508
|CLNHGVS=NC_000012.11:g.110252547G>A
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605427.0012
|COMMON=1
|Disease=Sodium serum level quantitative trait locus 1
|FwdALT=T
|FwdREF=C
|GENEINFO=TRPV4:59341
|GENE_ID=59341
|GENE_NAME=TRPV4
|REF=G
|RSPOS=110252547
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05016000000015051f110101
|WGT=0
|dbSNPBuildID=107
|rsid=3742030
}}

{{on chip | HumanOmni1Quad}}