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rs80356711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356711(C;T)
Make rs80356711(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4699698
GenePRNP
is asnp
is mentioned by
dbSNPrs80356711
ebirs80356711
HLIrs80356711
Exacrs80356711
Varsomers80356711
Maprs80356711
PheGenIrs80356711
hapmaprs80356711
1000 genomesrs80356711
hgdprs80356711
ensemblrs80356711
gopubmedrs80356711
geneviewrs80356711
scholarrs80356711
googlers80356711
pharmgkbrs80356711
gwascentralrs80356711
openSNPrs80356711
23andMers80356711
23andMe allrs80356711
SNP Nexus

SNPshotrs80356711
SNPdbers80356711
MSV3drs80356711
GWAS Ctlgrs80356711
Max Magnitude0
ClinVar
Risk rs80356711(T;T)
Alt rs80356711(T;T)
Reference rs80356711(C;C)
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.4680344C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000020246.1, RCV000074470.14,