{{Rsnum
|rsid=121918351
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=JAG1
|position=10658611
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=JAG1
}}{{omim
|id=601920
|rsnum=121918351
|variant=0006
}}{{ClinVar
|rsid=121918351
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=10639259
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=JAG1:182
|GENE_NAME=JAG1
|GENE_ID=182
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.10639259C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601920.0006
|CLNSIG=5
|CLNCUI=C1956125
|CLNDBN=Alagille syndrome 1
|Disease=Alagille syndrome 1
|CLNACC=RCV000008059.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1273:C1956125:118450:52
}}