rs864622781

Orientation

plus

Stabilized

plus

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

Make rs864622781(G;T)

Make rs864622781(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

122488926

Gene	HTRA1, LOC105378526

is a	snp
is	mentioned by
dbSNP	rs864622781
dbSNP (classic)	rs864622781
ClinGen	rs864622781
ebi	rs864622781
HLI	rs864622781
Exac	rs864622781
Gnomad	rs864622781
Varsome	rs864622781
LitVar	rs864622781
Map	rs864622781
PheGenI	rs864622781
Biobank	rs864622781
1000 genomes	rs864622781
hgdp	rs864622781
ensembl	rs864622781
geneview	rs864622781
scholar	rs864622781
google	rs864622781
pharmgkb	rs864622781
gwascentral	rs864622781
openSNP	rs864622781
23andMe	rs864622781
SNPshot	rs864622781
SNPdbe	rs864622781
MSV3d	rs864622781
GWAS Ctlg	rs864622781

Max Magnitude

0

ClinVar
Risk	rs864622781(T;T)
Alt	rs864622781(T;T)
Reference	Rs864622781(G;G)
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.124248442G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000206925.2,