rs137852642

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs137852642(C;T)

Make rs137852642(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

15192242

Gene

NOTCH3

is a	snp
is	mentioned by
dbSNP	rs137852642
dbSNP (classic)	rs137852642
ClinGen	rs137852642
ebi	rs137852642
HLI	rs137852642
Exac	rs137852642
Gnomad	rs137852642
Varsome	rs137852642
LitVar	rs137852642
Map	rs137852642
PheGenI	rs137852642
Biobank	rs137852642
1000 genomes	rs137852642
hgdp	rs137852642
ensembl	rs137852642
geneview	rs137852642
scholar	rs137852642
google	rs137852642
pharmgkb	rs137852642
gwascentral	rs137852642
openSNP	rs137852642
23andMe	rs137852642
SNPshot	rs137852642
SNPdbe	rs137852642
MSV3d	rs137852642
GWAS Ctlg	rs137852642

Max Magnitude

0

OMIM	600276
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137852642(A;A) rs137852642(T;T)
Alt	rs137852642(A;A) rs137852642(T;T)
Reference	Rs137852642(C;C)
Significance	Pathogenic
Disease	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Recurrent subcortical infarcts
Variation	info
Gene	NOTCH3
CLNDBN	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Recurrent subcortical infarcts
Reversed	1
HGVS	NC_000019.9:g.15303053G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009806.3, RCV000415016.1,