rs398122370

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs398122370(C;C)

Make rs398122370(C;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

4699851

Gene

PRNP

is a	snp
is	mentioned by
dbSNP	rs398122370
dbSNP (classic)	rs398122370
ClinGen	rs398122370
ebi	rs398122370
HLI	rs398122370
Exac	rs398122370
Gnomad	rs398122370
Varsome	rs398122370
LitVar	rs398122370
Map	rs398122370
PheGenI	rs398122370
Biobank	rs398122370
1000 genomes	rs398122370
hgdp	rs398122370
ensembl	rs398122370
geneview	rs398122370
scholar	rs398122370
google	rs398122370
pharmgkb	rs398122370
gwascentral	rs398122370
openSNP	rs398122370
23andMe	rs398122370
SNPshot	rs398122370
SNPdbe	rs398122370
MSV3d	rs398122370
GWAS Ctlg	rs398122370

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000074468.15,