{{Rsnum
|rsid=121434345
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CHD7
|position=60741596
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHD7
}}{{omim
|id=608892
|rsnum=121434345
|variant=0015
}}{{ClinVar
|rsid=121434345
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=61654155
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CHD7:55636
|GENE_NAME=CHD7
|GENE_ID=55636
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.61654155A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608892.0015
|CLNSIG=5
|CLNCUI=C2675302
|CLNDBN=Kallmann syndrome 5
|Disease=Kallmann syndrome 5
|CLNACC=RCV000002116.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1334:C2675302:612370:478
}}