rs80356710

Orientation

plus

Stabilized

plus

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

Make rs80356710(G;G)

Make rs80356710(G;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

4699655

Gene

PRNP

is a	snp
is	mentioned by
dbSNP	rs80356710
dbSNP (classic)	rs80356710
ClinGen	rs80356710
ebi	rs80356710
HLI	rs80356710
Exac	rs80356710
Gnomad	rs80356710
Varsome	rs80356710
LitVar	rs80356710
Map	rs80356710
PheGenI	rs80356710
Biobank	rs80356710
1000 genomes	rs80356710
hgdp	rs80356710
ensembl	rs80356710
geneview	rs80356710
scholar	rs80356710
google	rs80356710
pharmgkb	rs80356710
gwascentral	rs80356710
openSNP	rs80356710
23andMe	rs80356710
SNPshot	rs80356710
SNPdbe	rs80356710
MSV3d	rs80356710
GWAS Ctlg	rs80356710

Max Magnitude

0

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,