Have questions? Visit https://www.reddit.com/r/SNPedia

rs730566

From SNPedia

Orientationminus
Stabilizedminus
Make rs730566(G;G)
Make rs730566(G;T)
Make rs730566(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position48445644
GeneATRIP
is asnp
is mentioned by
dbSNPrs730566
ebirs730566
HLIrs730566
Exacrs730566
Varsomers730566
Maprs730566
PheGenIrs730566
hapmaprs730566
1000 genomesrs730566
hgdprs730566
ensemblrs730566
gopubmedrs730566
geneviewrs730566
scholarrs730566
googlers730566
pharmgkbrs730566
gwascentralrs730566
openSNPrs730566
23andMers730566
23andMe allrs730566
SNP Nexus

SNPshotrs730566
SNPdbers730566
MSV3drs730566
GWAS Ctlgrs730566
GMAF0.3384
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22210626OA-icon.png]
Trait
Title Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Risk Allele
P-val 0.000007
Odds Ratio 1.2700 None