rs587776873

Orientation

plus

Stabilized

plus

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

Make rs587776873(A;A)

Make rs587776873(A;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

122506796

Gene

HTRA1

is a	snp
is	mentioned by
dbSNP	rs587776873
dbSNP (classic)	rs587776873
ClinGen	rs587776873
ebi	rs587776873
HLI	rs587776873
Exac	rs587776873
Gnomad	rs587776873
Varsome	rs587776873
LitVar	rs587776873
Map	rs587776873
PheGenI	rs587776873
Biobank	rs587776873
1000 genomes	rs587776873
hgdp	rs587776873
ensembl	rs587776873
geneview	rs587776873
scholar	rs587776873
google	rs587776873
pharmgkb	rs587776873
gwascentral	rs587776873
openSNP	rs587776873
23andMe	rs587776873
SNPshot	rs587776873
SNPdbe	rs587776873
MSV3d	rs587776873
GWAS Ctlg	rs587776873

Max Magnitude

0

ClinVar
Risk	rs587776873(A;A) rs587776873(C;C)
Alt	rs587776873(A;A) rs587776873(C;C)
Reference	Rs587776873(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.124266312G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023168.7,