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rs587776445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776445(A;A)
Make rs587776445(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position122506734
GeneHTRA1
is asnp
is mentioned by
dbSNPrs587776445
ebirs587776445
HLIrs587776445
Exacrs587776445
Varsomers587776445
Maprs587776445
PheGenIrs587776445
hapmaprs587776445
1000 genomesrs587776445
hgdprs587776445
ensemblrs587776445
gopubmedrs587776445
geneviewrs587776445
scholarrs587776445
googlers587776445
pharmgkbrs587776445
gwascentralrs587776445
openSNPrs587776445
23andMers587776445
23andMe allrs587776445
SNP Nexus

SNPshotrs587776445
SNPdbers587776445
MSV3drs587776445
GWAS Ctlgrs587776445
Max Magnitude0
ClinVar
Risk rs587776445(A;A)
Alt rs587776445(A;A)
Reference rs587776445(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.124266250G>A
CLNSRC ClinVar
CLNACC RCV000144147.1,