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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
ebirs4699052
HLIrs4699052
Exacrs4699052
Varsomers4699052
Maprs4699052
PheGenIrs4699052
hapmaprs4699052
1000 genomesrs4699052
hgdprs4699052
ensemblrs4699052
gopubmedrs4699052
geneviewrs4699052
scholarrs4699052
googlers4699052
pharmgkbrs4699052
gwascentralrs4699052
openSNPrs4699052
23andMers4699052
23andMe allrs4699052
SNP Nexus

SNPshotrs4699052
SNPdbers4699052
MSV3drs4699052
GWAS Ctlgrs4699052
GMAF0.4279
Max Magnitude
? (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]


GET Evidence
rs4699052
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.453125
summary