{{Rsnum
|rsid=387906271
|Chromosome=8
|position=60801598
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CHD7
|Gene_s=CHD7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=8
|CLNACC=RCV000002113.1; RCV000002114.1
|CLNALLE=1
|CLNDBN=CHARGE association; Kallmann syndrome 5
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1117:C0265354:214800:138:47535005; NBK1334:C2675302:612370:478
|CLNHGVS=NC_000008.10:g.61714157G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608892.0013
|Disease=CHARGE association; Kallmann syndrome 5
|FwdALT=C
|FwdREF=G
|REF=G
|RSPOS=61714157
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906271
|GENEINFO=CHD7:55636
|GENE_ID=55636
|GENE_NAME=CHD7
}}