rs781563777

Orientation

plus

Stabilized

plus

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

Make rs781563777(A;A)

Make rs781563777(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

122488946

Gene	HTRA1, LOC105378526

is a	snp
is	mentioned by
dbSNP	rs781563777
dbSNP (classic)	rs781563777
ClinGen	rs781563777
ebi	rs781563777
HLI	rs781563777
Exac	rs781563777
Gnomad	rs781563777
Varsome	rs781563777
LitVar	rs781563777
Map	rs781563777
PheGenI	rs781563777
Biobank	rs781563777
1000 genomes	rs781563777
hgdp	rs781563777
ensembl	rs781563777
geneview	rs781563777
scholar	rs781563777
google	rs781563777
pharmgkb	rs781563777
gwascentral	rs781563777
openSNP	rs781563777
23andMe	rs781563777
SNPshot	rs781563777
SNPdbe	rs781563777
MSV3d	rs781563777
GWAS Ctlg	rs781563777

Max Magnitude

0

ClinVar
Risk	rs781563777(A;A) rs781563777(C;C) rs781563777(T;T)
Alt	rs781563777(A;A) rs781563777(C;C) rs781563777(T;T)
Reference	Rs781563777(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.124248462G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000206984.2,