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rs398122370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122370(C;C)
Make rs398122370(C;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position4699851
GenePRNP
is asnp
is mentioned by
dbSNPrs398122370
ebirs398122370
HLIrs398122370
Exacrs398122370
Varsomers398122370
Maprs398122370
PheGenIrs398122370
hapmaprs398122370
1000 genomesrs398122370
hgdprs398122370
ensemblrs398122370
gopubmedrs398122370
geneviewrs398122370
scholarrs398122370
googlers398122370
pharmgkbrs398122370
gwascentralrs398122370
openSNPrs398122370
23andMers398122370
23andMe allrs398122370
SNP Nexus

SNPshotrs398122370
SNPdbers398122370
MSV3drs398122370
GWAS Ctlgrs398122370
Max Magnitude0
ClinVar
Risk rs398122370(C;C)
Alt rs398122370(C;C)
Reference rs398122370(G;G)
Significance Pathogenic
Disease Jakob-Creutzfeldt disease
Variation info
Gene PRNP
CLNDBN Jakob-Creutzfeldt disease
Reversed 0
HGVS NC_000020.10:g.4680497G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000074468.15,