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rs864622781

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622781(G;T)
Make rs864622781(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position122488926
GeneHTRA1, LOC105378526
is asnp
is mentioned by
dbSNPrs864622781
ebirs864622781
HLIrs864622781
Exacrs864622781
Varsomers864622781
Maprs864622781
PheGenIrs864622781
hapmaprs864622781
1000 genomesrs864622781
hgdprs864622781
ensemblrs864622781
gopubmedrs864622781
geneviewrs864622781
scholarrs864622781
googlers864622781
pharmgkbrs864622781
gwascentralrs864622781
openSNPrs864622781
23andMers864622781
23andMe allrs864622781
SNP Nexus

SNPshotrs864622781
SNPdbers864622781
MSV3drs864622781
GWAS Ctlgrs864622781
Max Magnitude0
ClinVar
Risk rs864622781(T;T)
Alt rs864622781(T;T)
Reference rs864622781(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.124248442G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000206925.1,