{{Rsnum
|rsid=137852641
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NOTCH3
|position=15191466
|Gene_s=NOTCH3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600276
|variant=0007
|rsnum=137852641
}}{{ClinVar
|rsid=137852641
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=15302277
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NOTCH3:4854
|GENE_NAME=NOTCH3
|GENE_ID=4854
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.15302277G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600276.0007
|CLNSIG=5
|CLNCUI=C1272305
|CLNDBN=Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|Disease=Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
|CLNACC=RCV000009805.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1500:C1272305:125310:136:390936003
}}