rs587776446

Orientation

plus

Stabilized

plus

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

Make rs587776446(C;T)

Make rs587776446(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

122506767

Gene

HTRA1

is a	snp
is	mentioned by
dbSNP	rs587776446
dbSNP (classic)	rs587776446
ClinGen	rs587776446
ebi	rs587776446
HLI	rs587776446
Exac	rs587776446
Gnomad	rs587776446
Varsome	rs587776446
LitVar	rs587776446
Map	rs587776446
PheGenI	rs587776446
Biobank	rs587776446
1000 genomes	rs587776446
hgdp	rs587776446
ensembl	rs587776446
geneview	rs587776446
scholar	rs587776446
google	rs587776446
pharmgkb	rs587776446
gwascentral	rs587776446
openSNP	rs587776446
23andMe	rs587776446
SNPshot	rs587776446
SNPdbe	rs587776446
MSV3d	rs587776446
GWAS Ctlg	rs587776446

Max Magnitude

0

ClinVar
Risk	rs587776446(T;T)
Alt	rs587776446(T;T)
Reference	Rs587776446(C;C)
Significance	Other
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.124266283C>T
CLNSRC	ClinVar
CLNACC	RCV000144148.1,