rs12761224

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs12761224(G;T)

Make rs12761224(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

70767761

is a	snp
is	mentioned by
dbSNP	rs12761224
dbSNP (classic)	rs12761224
ClinGen	rs12761224
ebi	rs12761224
HLI	rs12761224
Exac	rs12761224
Gnomad	rs12761224
Varsome	rs12761224
LitVar	rs12761224
Map	rs12761224
PheGenI	rs12761224
Biobank	rs12761224
1000 genomes	rs12761224
hgdp	rs12761224
ensembl	rs12761224
geneview	rs12761224
scholar	rs12761224
google	rs12761224
pharmgkb	rs12761224
gwascentral	rs12761224
openSNP	rs12761224
23andMe	rs12761224
SNPshot	rs12761224
SNPdbe	rs12761224
MSV3d	rs12761224
GWAS Ctlg	rs12761224

GMAF

0.07713

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

GWAS snp
PMID	[PMID 22210626]
Trait
Title	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Risk Allele
P-val	0.000006
Odds Ratio	1.3861 None