rs587776448

Orientation

plus

Stabilized

plus

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

Make rs587776448(-;-)

Make rs587776448(-;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

122461778

Gene	HTRA1, LOC105378525

is a	snp
is	mentioned by
dbSNP	rs587776448
dbSNP (classic)	rs587776448
ClinGen	rs587776448
ebi	rs587776448
HLI	rs587776448
Exac	rs587776448
Gnomad	rs587776448
Varsome	rs587776448
LitVar	rs587776448
Map	rs587776448
PheGenI	rs587776448
Biobank	rs587776448
1000 genomes	rs587776448
hgdp	rs587776448
ensembl	rs587776448
geneview	rs587776448
scholar	rs587776448
google	rs587776448
pharmgkb	rs587776448
gwascentral	rs587776448
openSNP	rs587776448
23andMe	rs587776448
SNPshot	rs587776448
SNPdbe	rs587776448
MSV3d	rs587776448
GWAS Ctlg	rs587776448

Max Magnitude

0

ClinVar
Risk	rs587776448(-;-)
Alt	rs587776448(-;-)
Reference	Rs587776448(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.124221294delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144150.1, RCV000157766.5,