{{Rsnum
|rsid=104894749
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AVPR2
|position=153906120
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AVPR2
}}{{omim
|id=300538
|rsnum=104894749
|variant=0004
}}{{ClinVar
|rsid=104894749
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=153171574
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=AVPR2:554
|GENE_NAME=AVPR2
|GENE_ID=554
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153171574A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300538.0004
|CLNSIG=5
|CLNCUI=C1563705
|CLNDBN=Nephrogenic diabetes insipidus, X-linked; Nephrogenic diabetes insipidus
|Disease=Nephrogenic diabetes insipidus; Nephrogenic diabetes insipidus
|CLNACC=RCV000011585.1; RCV000029393.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:SNOMED_CT
|CLNDSDBID=NBK1177:C1563705:304800:223; C0162283:111395007
}}{{PMID Auto
|PMID=1303257
|Title=Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus.
}}

{{PMID Auto
|PMID=7833930
|Title=Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidus.
}}

{{PMID Auto
|PMID=7913579
|Title=Heterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus.
|OA=1
}}

{{PMID Auto
|PMID=10770218
|Title=Functional characterization of the molecular defects causing nephrogenic diabetes insipidus in eight families.
}}

{{PMID Auto
|PMID=11128419
|Title=Nephrogenic diabetes insipidus.
}}

{{PMID Auto
|PMID=17216256
|Title=A case of nephrogenic diabetes insipidus with a novel missense mutation in the AVPR2 gene.
}}