{{Rsnum
|rsid=121434627
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SCN1B
|position=35033550
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN1B
}}{{omim
|id=600235
|rsnum=121434627
|variant=0004
}}{{ClinVar
|rsid=121434627
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=35524454
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN1B:6324
|GENE_NAME=SCN1B
|GENE_ID=6324
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.35524454G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000009837.1
|CLNDBN=Cardiac conduction defect, nonspecific
|CLNDSDB=MedGen
|CLNDSDBID=C2748542
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600235.0004
|Disease=Cardiac conduction defect
}}