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

rs864622783

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622783(A;A)
Make rs864622783(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position122507369
GeneHTRA1
is asnp
is mentioned by
dbSNPrs864622783
ebirs864622783
HLIrs864622783
Exacrs864622783
Varsomers864622783
Maprs864622783
PheGenIrs864622783
hapmaprs864622783
1000 genomesrs864622783
hgdprs864622783
ensemblrs864622783
gopubmedrs864622783
geneviewrs864622783
scholarrs864622783
googlers864622783
pharmgkbrs864622783
gwascentralrs864622783
openSNPrs864622783
23andMers864622783
23andMe allrs864622783
SNP Nexus

SNPshotrs864622783
SNPdbers864622783
MSV3drs864622783
GWAS Ctlgrs864622783
Max Magnitude0
ClinVar
Risk rs864622783(A;A)
Alt rs864622783(A;A)
Reference rs864622783(G;G)
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.124266885G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000206946.1,