rs587776445

Orientation

plus

Stabilized

plus

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

Make rs587776445(A;A)

Make rs587776445(A;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

122506734

Gene

HTRA1

is a	snp
is	mentioned by
dbSNP	rs587776445
dbSNP (classic)	rs587776445
ClinGen	rs587776445
ebi	rs587776445
HLI	rs587776445
Exac	rs587776445
Gnomad	rs587776445
Varsome	rs587776445
LitVar	rs587776445
Map	rs587776445
PheGenI	rs587776445
Biobank	rs587776445
1000 genomes	rs587776445
hgdp	rs587776445
ensembl	rs587776445
geneview	rs587776445
scholar	rs587776445
google	rs587776445
pharmgkb	rs587776445
gwascentral	rs587776445
openSNP	rs587776445
23andMe	rs587776445
SNPshot	rs587776445
SNPdbe	rs587776445
MSV3d	rs587776445
GWAS Ctlg	rs587776445

Max Magnitude

0

ClinVar
Risk	rs587776445(A;A)
Alt	rs587776445(A;A)
Reference	Rs587776445(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.124266250G>A
CLNSRC	ClinVar
CLNACC	RCV000144147.1,