rs80356711

Orientation

plus

Stabilized

plus

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

Make rs80356711(C;T)

Make rs80356711(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

4699698

Gene

PRNP

is a	snp
is	mentioned by
dbSNP	rs80356711
dbSNP (classic)	rs80356711
ClinGen	rs80356711
ebi	rs80356711
HLI	rs80356711
Exac	rs80356711
Gnomad	rs80356711
Varsome	rs80356711
LitVar	rs80356711
Map	rs80356711
PheGenI	rs80356711
Biobank	rs80356711
1000 genomes	rs80356711
hgdp	rs80356711
ensembl	rs80356711
geneview	rs80356711
scholar	rs80356711
google	rs80356711
pharmgkb	rs80356711
gwascentral	rs80356711
openSNP	rs80356711
23andMe	rs80356711
SNPshot	rs80356711
SNPdbe	rs80356711
MSV3d	rs80356711
GWAS Ctlg	rs80356711

Max Magnitude

0

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,