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rs864622782

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622782(A;A)
Make rs864622782(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position122506765
GeneHTRA1
is asnp
is mentioned by
dbSNPrs864622782
ebirs864622782
HLIrs864622782
Exacrs864622782
Varsomers864622782
Maprs864622782
PheGenIrs864622782
hapmaprs864622782
1000 genomesrs864622782
hgdprs864622782
ensemblrs864622782
gopubmedrs864622782
geneviewrs864622782
scholarrs864622782
googlers864622782
pharmgkbrs864622782
gwascentralrs864622782
openSNPrs864622782
23andMers864622782
23andMe allrs864622782
SNP Nexus

SNPshotrs864622782
SNPdbers864622782
MSV3drs864622782
GWAS Ctlgrs864622782
Max Magnitude0
ClinVar
Risk rs864622782(A;A)
Alt rs864622782(A;A)
Reference rs864622782(C;C)
Significance Pathogenic
Disease Cerebral arteriopathy
Variation info
Gene HTRA1
CLNDBN Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Reversed 0
HGVS NC_000010.10:g.124266281C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000206899.1,