rs864622782

Orientation

plus

Stabilized

plus

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

Make rs864622782(A;A)

Make rs864622782(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

122506765

Gene

HTRA1

is a	snp
is	mentioned by
dbSNP	rs864622782
dbSNP (classic)	rs864622782
ClinGen	rs864622782
ebi	rs864622782
HLI	rs864622782
Exac	rs864622782
Gnomad	rs864622782
Varsome	rs864622782
LitVar	rs864622782
Map	rs864622782
PheGenI	rs864622782
Biobank	rs864622782
1000 genomes	rs864622782
hgdp	rs864622782
ensembl	rs864622782
geneview	rs864622782
scholar	rs864622782
google	rs864622782
pharmgkb	rs864622782
gwascentral	rs864622782
openSNP	rs864622782
23andMe	rs864622782
SNPshot	rs864622782
SNPdbe	rs864622782
MSV3d	rs864622782
GWAS Ctlg	rs864622782

Max Magnitude

0

ClinVar
Risk	rs864622782(A;A)
Alt	rs864622782(A;A)
Reference	Rs864622782(C;C)
Significance	Pathogenic
Disease	Cerebral arteriopathy
Variation	info
Gene	HTRA1
CLNDBN	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Reversed	0
HGVS	NC_000010.10:g.124266281C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000206899.2,