rs28933698

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;T)	7.7	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 (CADASIL)
(T;T)	0	common in clinvar

Make rs28933698(C;C)

Reference

GRCh38 38.1/141

Chromosome

19

Position

15189004

Gene

NOTCH3

is a	snp
is	mentioned by
dbSNP	rs28933698
dbSNP (classic)	rs28933698
ClinGen	rs28933698
ebi	rs28933698
HLI	rs28933698
Exac	rs28933698
Gnomad	rs28933698
Varsome	rs28933698
LitVar	rs28933698
Map	rs28933698
PheGenI	rs28933698
Biobank	rs28933698
1000 genomes	rs28933698
hgdp	rs28933698
ensembl	rs28933698
geneview	rs28933698
scholar	rs28933698
google	rs28933698
pharmgkb	rs28933698
gwascentral	rs28933698
openSNP	rs28933698
23andMe	rs28933698
SNPshot	rs28933698
SNPdbe	rs28933698
MSV3d	rs28933698
GWAS Ctlg	rs28933698

Max Magnitude

7.7

OMIM	600276
Desc	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY
Variant	0006
Related	also

ClinVar
Risk	rs28933698(C;C)
Alt	rs28933698(C;C)
Reference	Rs28933698(T;T)
Significance	Pathogenic
Disease	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Variation	info
Gene	NOTCH3
CLNDBN	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Reversed	1
HGVS	NC_000019.9:g.15299815A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009804.6,