{{Rsnum
|rsid=121918353
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=JAG1
|position=10656452
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=JAG1
}}{{omim
|id=601920
|rsnum=121918353
|variant=0012
}}{{ClinVar
|rsid=121918353
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=10637100
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=JAG1:182
|GENE_NAME=JAG1
|GENE_ID=182
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.10637100C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000008065.1
|CLNDBN=Deafness, congenital heart defects, and posterior embryotoxon
|CLNDSDB=MedGen
|CLNDSDBID=C1866053
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601920.0012
|Disease=Deafness
}}