{{Rsnum
|rsid=104894761
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AVPR2
|position=153905915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AVPR2
}}{{omim
|id=300538
|rsnum=104894761
|variant=0021
}}{{ClinVar
|rsid=104894761
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=153171369
|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; 2
|CLNHGVS=NC_000023.10:g.153171369C>G; NC_000023.10:g.153171369C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300538.0021
|CLNSIG=5
|CLNCUI=C1845202
|CLNDBN=Nephrogenic diabetes insipidus; Nephrogenic syndrome of inappropriate antidiuresis
|Disease=Nephrogenic diabetes insipidus; Nephrogenic syndrome of inappropriate antidiuresis
|CLNACC=RCV000029389.1; RCV000011601.9
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0162283:111395007; C1845202:300539:93606
}}{{PMID Auto
|PMID=19812297
|Title=Diverse vasopressin V2 receptor functionality underlying partial congenital nephrogenic diabetes insipidus.
}}