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rs2903698

From SNPedia

Orientationplus
Stabilizedplus
Make rs2903698(A;A)
Make rs2903698(A;G)
Make rs2903698(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position75407765
is asnp
is mentioned by
dbSNPrs2903698
ebirs2903698
HLIrs2903698
Exacrs2903698
Varsomers2903698
Maprs2903698
PheGenIrs2903698
hapmaprs2903698
1000 genomesrs2903698
hgdprs2903698
ensemblrs2903698
gopubmedrs2903698
geneviewrs2903698
scholarrs2903698
googlers2903698
pharmgkbrs2903698
gwascentralrs2903698
openSNPrs2903698
23andMers2903698
23andMe allrs2903698
SNP Nexus

SNPshotrs2903698
SNPdbers2903698
MSV3drs2903698
GWAS Ctlgrs2903698
GMAF0.1566
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio 1.2528 None