{{Rsnum
|rsid = 28937321
|Gene = NOTCH3
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=19
|position=15192504
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NOTCH3
}}{{omim
|desc=CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY
|id=600276
|rsnum=28937321
|variant=0001
}}
{{ neighbor
| rsid = 28933696
| distance = 370
}}{{ClinVar
|rsid=28937321
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=15303315
|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.15303315C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600276.0001
|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=RCV000009799.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1500:C1272305:125310:136:390936003
}}

{{on chip | 23andMe v4}}