rs137852641

Orientation

minus

Stabilized

minus

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

Make rs137852641(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

15191466

Gene

NOTCH3

is a	snp
is	mentioned by
dbSNP	rs137852641
dbSNP (classic)	rs137852641
ClinGen	rs137852641
ebi	rs137852641
HLI	rs137852641
Exac	rs137852641
Gnomad	rs137852641
Varsome	rs137852641
LitVar	rs137852641
Map	rs137852641
PheGenI	rs137852641
Biobank	rs137852641
1000 genomes	rs137852641
hgdp	rs137852641
ensembl	rs137852641
geneview	rs137852641
scholar	rs137852641
google	rs137852641
pharmgkb	rs137852641
gwascentral	rs137852641
openSNP	rs137852641
23andMe	rs137852641
SNPshot	rs137852641
SNPdbe	rs137852641
MSV3d	rs137852641
GWAS Ctlg	rs137852641

Max Magnitude

7.7

OMIM	600276
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137852641(T;T)
Alt	rs137852641(T;T)
Reference	Rs137852641(C;C)
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.15302277G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009805.6,