{{Rsnum
|rsid=151340626
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CLCN5
|position=50085987
|Gene_s=CLCN5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=151340626
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=49850644
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=CLCN5:1184
|GENE_NAME=CLCN5
|GENE_ID=1184
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.49850644C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK99494; 300008.0007
|CLNSIG=5
|CLNCUI=C1845168
|CLNDBN=X-linked recessive hypophosphatemic rickets
|Disease=X-linked recessive hypophosphatemic rickets
|CLNACC=RCV000012570.23
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK99494:C1845168:300554:1652:93622
}}