rs78501403

Orientation

plus

Stabilized

plus

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

Make rs78501403(C;G)

Make rs78501403(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

15174125

Gene

NOTCH3

is a	snp
is	mentioned by
dbSNP	rs78501403
dbSNP (classic)	rs78501403
ClinGen	rs78501403
ebi	rs78501403
HLI	rs78501403
Exac	rs78501403
Gnomad	rs78501403
Varsome	rs78501403
LitVar	rs78501403
Map	rs78501403
PheGenI	rs78501403
Biobank	rs78501403
1000 genomes	rs78501403
hgdp	rs78501403
ensembl	rs78501403
geneview	rs78501403
scholar	rs78501403
google	rs78501403
pharmgkb	rs78501403
gwascentral	rs78501403
openSNP	rs78501403
23andMe	rs78501403
SNPshot	rs78501403
SNPdbe	rs78501403
MSV3d	rs78501403
GWAS Ctlg	rs78501403

GMAF

0.003214

Max Magnitude

0

[PMID 24086431] NOTCH3 Variants and Risk of Ischemic Stroke

ClinVar
Risk	rs78501403(G;G) rs78501403(T;T)
Alt	rs78501403(G;G) rs78501403(T;T)
Reference	Rs78501403(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Variation	info
Gene	NOTCH3
CLNDBN	not specified Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Reversed	0
HGVS	NC_000019.9:g.15284936C>G
CLNSRC
CLNACC	RCV000253764.1, RCV000392209.1,