{{Rsnum
|rsid=387907576
|Chromosome=16
|position=1461460
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLCN7
|Gene_s=CLCN7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000050235.1; RCV000055847.1
|CLNALLE=1
|CLNDBN=Osteopetrosis autosomal dominant type 2; Osteopetrosis autosomal recessive 4
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1127:C1833700:166600:53; NBK1127:C1969106:611490:667
|CLNHGVS=NC_000016.9:g.1511461T>C
|CLNORIGIN=4
|CLNSIG=5
|Disease=Osteopetrosis autosomal dominant type 2; Osteopetrosis autosomal recessive 4
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=1511461
|Reversed=1
|SAO=3
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907576
|CLNSRC=GeneReviews
|CLNSRCID=NBK1127
|GENEINFO=CLCN7:1186
|GENE_ID=1186
|GENE_NAME=CLCN7
}}