Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776446(C;T)
Make rs587776446(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position122506767
GeneHTRA1
is asnp
is mentioned by
dbSNPrs587776446
ebirs587776446
HLIrs587776446
Exacrs587776446
Varsomers587776446
Maprs587776446
PheGenIrs587776446
hapmaprs587776446
1000 genomesrs587776446
hgdprs587776446
ensemblrs587776446
gopubmedrs587776446
geneviewrs587776446
scholarrs587776446
googlers587776446
pharmgkbrs587776446
gwascentralrs587776446
openSNPrs587776446
23andMers587776446
23andMe allrs587776446
SNP Nexus

SNPshotrs587776446
SNPdbers587776446
MSV3drs587776446
GWAS Ctlgrs587776446
Max Magnitude0
ClinVar
Risk rs587776446(T;T)
Alt rs587776446(T;T)
Reference rs587776446(C;C)
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.124266283C>T
CLNSRC ClinVar
CLNACC RCV000144148.1,