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rs781563777

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781563777(A;A)
Make rs781563777(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position122488946
GeneHTRA1, LOC105378526
is asnp
is mentioned by
dbSNPrs781563777
ebirs781563777
HLIrs781563777
Exacrs781563777
Varsomers781563777
Maprs781563777
PheGenIrs781563777
hapmaprs781563777
1000 genomesrs781563777
hgdprs781563777
ensemblrs781563777
gopubmedrs781563777
geneviewrs781563777
scholarrs781563777
googlers781563777
pharmgkbrs781563777
gwascentralrs781563777
openSNPrs781563777
23andMers781563777
23andMe allrs781563777
SNP Nexus

SNPshotrs781563777
SNPdbers781563777
MSV3drs781563777
GWAS Ctlgrs781563777
Max Magnitude0
ClinVar
Risk rs781563777(A,T;A,T)
Alt rs781563777(A,T;A,T)
Reference rs781563777(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.124248462G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000206984.1,