rs35769976

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(G;G)	0	common in clinvar

Make rs35769976(C;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

15180765

Gene	MIR6795, NOTCH3

is a	snp
is	mentioned by
dbSNP	rs35769976
dbSNP (classic)	rs35769976
ClinGen	rs35769976
ebi	rs35769976
HLI	rs35769976
Exac	rs35769976
Gnomad	rs35769976
Varsome	rs35769976
LitVar	rs35769976
Map	rs35769976
PheGenI	rs35769976
Biobank	rs35769976
1000 genomes	rs35769976
hgdp	rs35769976
ensembl	rs35769976
geneview	rs35769976
scholar	rs35769976
google	rs35769976
pharmgkb	rs35769976
gwascentral	rs35769976
openSNP	rs35769976
23andMe	rs35769976
SNPshot	rs35769976
SNPdbe	rs35769976
MSV3d	rs35769976
GWAS Ctlg	rs35769976

GMAF

0.08356

Max Magnitude

0

OMIM	600276
Desc	NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3
Variant
Related	also

OMIM	600276
Desc
Variant	0010
Related	also

ClinVar
Risk	rs35769976(A;A) Rs35769976(G;G) rs35769976(T;T)
Alt	rs35769976(A;A) Rs35769976(G;G) rs35769976(T;T)
Reference	Rs35769976(C;C)
Significance	Other
Disease	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy not specified
Variation	info
Gene	NOTCH3 MIR6795
CLNDBN	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy not specified
Reversed	0
HGVS	NC_000019.9:g.15291576C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009808.4, RCV000243215.1,