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rs587776449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776449(A;A)
Make rs587776449(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position122506874
GeneHTRA1
is asnp
is mentioned by
dbSNPrs587776449
ebirs587776449
HLIrs587776449
Exacrs587776449
Varsomers587776449
Maprs587776449
PheGenIrs587776449
hapmaprs587776449
1000 genomesrs587776449
hgdprs587776449
ensemblrs587776449
gopubmedrs587776449
geneviewrs587776449
scholarrs587776449
googlers587776449
pharmgkbrs587776449
gwascentralrs587776449
openSNPrs587776449
23andMers587776449
23andMe allrs587776449
SNP Nexus

SNPshotrs587776449
SNPdbers587776449
MSV3drs587776449
GWAS Ctlgrs587776449
Max Magnitude0
ClinVar
Risk rs587776449(A;A)
Alt rs587776449(A;A)
Reference rs587776449(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.124266390G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144150.1, RCV000157765.4,