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rs80356710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80356710(G;G)
Make rs80356710(G;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4699655
GenePRNP
is asnp
is mentioned by
dbSNPrs80356710
ebirs80356710
HLIrs80356710
Exacrs80356710
Varsomers80356710
Maprs80356710
PheGenIrs80356710
hapmaprs80356710
1000 genomesrs80356710
hgdprs80356710
ensemblrs80356710
gopubmedrs80356710
geneviewrs80356710
scholarrs80356710
googlers80356710
pharmgkbrs80356710
gwascentralrs80356710
openSNPrs80356710
23andMers80356710
23andMe allrs80356710
SNP Nexus

SNPshotrs80356710
SNPdbers80356710
MSV3drs80356710
GWAS Ctlgrs80356710
Max Magnitude0
ClinVar
Risk rs80356710(G;G)
Alt rs80356710(G;G)
Reference rs80356710(T;T)
Significance Pathogenic
Disease Genetic prion diseases CEREBRAL AMYLOID ANGIOPATHY
Variation info
Gene PRNP
CLNDBN Genetic prion diseases CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED
Reversed 0
HGVS NC_000020.10:g.4680301T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000020245.1, RCV000074469.15,