{{Rsnum
|rsid=121434435
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CLCN7
|position=1447038
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLCN7
}}{{omim
|id=602727
|rsnum=121434435
|variant=0004
}}{{ClinVar
|rsid=121434435
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=1497039
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CLCN7:1186
|GENE_NAME=CLCN7
|GENE_ID=1186
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.1497039G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1127; 602727.0004
|CLNSIG=5
|CLNCUI=C1833700
|CLNDBN=Osteopetrosis autosomal dominant type 2; Osteopetrosis autosomal recessive 4
|Disease=Osteopetrosis autosomal dominant type 2; Osteopetrosis autosomal recessive 4
|CLNACC=RCV000007266.1; RCV000055846.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1127:C1833700:166600:53; NBK1127:C1969106:611490:667
}}