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rs587776873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776873(A;A)
Make rs587776873(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position122506796
GeneHTRA1
is asnp
is mentioned by
dbSNPrs587776873
ebirs587776873
HLIrs587776873
Exacrs587776873
Varsomers587776873
Maprs587776873
PheGenIrs587776873
hapmaprs587776873
1000 genomesrs587776873
hgdprs587776873
ensemblrs587776873
gopubmedrs587776873
geneviewrs587776873
scholarrs587776873
googlers587776873
pharmgkbrs587776873
gwascentralrs587776873
openSNPrs587776873
23andMers587776873
23andMe allrs587776873
SNP Nexus

SNPshotrs587776873
SNPdbers587776873
MSV3drs587776873
GWAS Ctlgrs587776873
Max Magnitude0
ClinVar
Risk rs587776873(A,C;A,C)
Alt rs587776873(A,C;A,C)
Reference rs587776873(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.124266312G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023168.6,