{{Rsnum
|rsid=104894485
|Chromosome=15
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HCN4
|position=73325378
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HCN4
}}{{omim
|id=605206
|rsnum=104894485
|variant=0003
}}{{ClinVar
|rsid=104894485
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=73617719
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HCN4:10021
|GENE_NAME=HCN4
|GENE_ID=10021
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.73617719C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605206.0003
|CLNSIG=5
|CLNCUI=C1834144
|CLNDBN=Sick sinus syndrome 2, autosomal dominant
|Disease=Sick sinus syndrome 2
|CLNACC=RCV000005483.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1834144:163800:166282
}}