{{Rsnum
|rsid=111033632
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NOTCH2
|position=119967555
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NOTCH2
}}{{omim
|id=600275
|rsnum=111033632
|variant=0002
}}{{ClinVar
|rsid=111033632
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=119967555
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000a05000002110100
|GENEINFO=NOTCH2:4853
|GENE_NAME=NOTCH2
|GENE_ID=4853
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.119967555C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_024408.3:c.1331G>A; NBK1273; 600275.0002
|CLNSIG=5
|CLNCUI=C1857761; C1857761
|CLNDBN=Alagille syndrome 2
|Disease=Alagille syndrome 2
|CLNACC=RCV000009811.3
|Tags=RV;PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1273:C1857761:610205:ORPHA52
}}