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rs398122414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122414(A;A)
Make rs398122414(A;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position4699898
GenePRNP
is asnp
is mentioned by
dbSNPrs398122414
ebirs398122414
HLIrs398122414
Exacrs398122414
Varsomers398122414
Maprs398122414
PheGenIrs398122414
hapmaprs398122414
1000 genomesrs398122414
hgdprs398122414
ensemblrs398122414
gopubmedrs398122414
geneviewrs398122414
scholarrs398122414
googlers398122414
pharmgkbrs398122414
gwascentralrs398122414
openSNPrs398122414
23andMers398122414
23andMe allrs398122414
SNP Nexus

SNPshotrs398122414
SNPdbers398122414
MSV3drs398122414
GWAS Ctlgrs398122414
Max Magnitude0
ClinVar
Risk rs398122414(A;A)
Alt rs398122414(A;A)
Reference rs398122414(C;C)
Significance Pathogenic
Disease CEREBRAL AMYLOID ANGIOPATHY
Variation info
Gene PRNP
CLNDBN CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
Reversed 0
HGVS NC_000020.10:g.4680544C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074471.17,