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rs587776448

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776448(-;-)
Make rs587776448(-;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position122461778
GeneHTRA1
is asnp
is mentioned by
dbSNPrs587776448
ebirs587776448
HLIrs587776448
Exacrs587776448
Varsomers587776448
Maprs587776448
PheGenIrs587776448
hapmaprs587776448
1000 genomesrs587776448
hgdprs587776448
ensemblrs587776448
gopubmedrs587776448
geneviewrs587776448
scholarrs587776448
googlers587776448
pharmgkbrs587776448
gwascentralrs587776448
openSNPrs587776448
23andMers587776448
23andMe allrs587776448
SNP Nexus

SNPshotrs587776448
SNPdbers587776448
MSV3drs587776448
GWAS Ctlgrs587776448
Max Magnitude0
ClinVar
Risk rs587776448(;)
Alt rs587776448(;)
Reference rs587776448(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.124221294delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000144150.1, RCV000157766.4,