rs587776449

Orientation

plus

Stabilized

plus

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

Make rs587776449(A;A)

Make rs587776449(A;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

122506874

Gene

HTRA1

is a	snp
is	mentioned by
dbSNP	rs587776449
dbSNP (classic)	rs587776449
ClinGen	rs587776449
ebi	rs587776449
HLI	rs587776449
Exac	rs587776449
Gnomad	rs587776449
Varsome	rs587776449
LitVar	rs587776449
Map	rs587776449
PheGenI	rs587776449
Biobank	rs587776449
1000 genomes	rs587776449
hgdp	rs587776449
ensembl	rs587776449
geneview	rs587776449
scholar	rs587776449
google	rs587776449
pharmgkb	rs587776449
gwascentral	rs587776449
openSNP	rs587776449
23andMe	rs587776449
SNPshot	rs587776449
SNPdbe	rs587776449
MSV3d	rs587776449
GWAS Ctlg	rs587776449

Max Magnitude

0

ClinVar
Risk	rs587776449(A;A)
Alt	rs587776449(A;A)
Reference	Rs587776449(G;G)
Significance	Pathogenic
Disease	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
Variation	info
Gene	HTRA1
CLNDBN	Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
Reversed	0
HGVS	NC_000010.10:g.124266390G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144150.1, RCV000157765.5,