{{Rsnum
|rsid=267606915
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=NOTCH3
|position=15189085
|Gene_s=NOTCH3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000009809.1
|CLNALLE=1
|CLNDBN=Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1500:C1272305:125310:136:390936003
|CLNHGVS=NC_000019.9:g.15299896A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600276.0011
|Disease=Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|FwdALT=A
|FwdREF=T
|GENEINFO=NOTCH3:4854
|GENE_ID=4854
|GENE_NAME=NOTCH3
|REF=A
|RSPOS=15299896
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606915
}}