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rs4699052

From SNPedia

Orientationplus
Stabilizedplus
Make rs4699052(C;C)
Make rs4699052(C;T)
Make rs4699052(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position103216633
is asnp
is mentioned by
dbSNPrs4699052
dbSNP (classic)rs4699052
ClinGenrs4699052
ebirs4699052
HLIrs4699052
Exacrs4699052
Gnomadrs4699052
Varsomers4699052
LitVarrs4699052
Maprs4699052
PheGenIrs4699052
Biobankrs4699052
1000 genomesrs4699052
hgdprs4699052
ensemblrs4699052
geneviewrs4699052
scholarrs4699052
googlers4699052
pharmgkbrs4699052
gwascentralrs4699052
openSNPrs4699052
23andMers4699052
SNPshotrs4699052
SNPdbers4699052
MSV3drs4699052
GWAS Ctlgrs4699052
GMAF0.4279
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 19483681OA-icon.png]
Trait Testicular germ cell tumor
Title A genome-wide association study of testicular germ cell tumor
Risk Allele C
P-val 2E-7
Odds Ratio 1.21 [1.05-1.39]