rs74315410

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	8	Gerstmann–Straussler–Scheinker syndrome

Make rs74315410(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

4699612

Gene

PRNP

is a	snp
is	mentioned by
dbSNP	rs74315410
dbSNP (classic)	rs74315410
ClinGen	rs74315410
ebi	rs74315410
HLI	rs74315410
Exac	rs74315410
Gnomad	rs74315410
Varsome	rs74315410
LitVar	rs74315410
Map	rs74315410
PheGenI	rs74315410
Biobank	rs74315410
1000 genomes	rs74315410
hgdp	rs74315410
ensembl	rs74315410
geneview	rs74315410
scholar	rs74315410
google	rs74315410
pharmgkb	rs74315410
gwascentral	rs74315410
openSNP	rs74315410
23andMe	rs74315410
SNPshot	rs74315410
SNPdbe	rs74315410
MSV3d	rs74315410
GWAS Ctlg	rs74315410

Max Magnitude

8

OMIM	176640
Desc
Variant	0021
Related	also

ClinVar
Risk	rs74315410(T;T)
Alt	rs74315410(T;T)
Reference	Rs74315410(G;G)
Significance	Pathogenic
Disease	Gerstmann-Straussler-Scheinker syndrome
Variation	info
Gene	PRNP
CLNDBN	Gerstmann-Straussler-Scheinker syndrome
Reversed	0
HGVS	NC_000020.10:g.4680258G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014351.25,