{{Rsnum
|rsid=267607029
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN1B
|position=35033828
|Gene_s=SCN1B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=19
|CLNACC=RCV000009838.1
|CLNALLE=1
|CLNDBN=Cardiac conduction defect, nonspecific
|CLNDSDB=MedGen
|CLNDSDBID=C2748542
|CLNHGVS=NC_000019.9:g.35524732G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600235.0005
|Disease=Cardiac conduction defect
|FwdALT=A
|FwdREF=G
|GENEINFO=SCN1B:6324
|GENE_ID=6324
|GENE_NAME=SCN1B
|REF=G
|RSPOS=35524732
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607029
}}