rs4699052
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4699052(C;C) |
Make rs4699052(C;T) |
Make rs4699052(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 103216633 |
is a | snp |
is | mentioned by |
dbSNP | rs4699052 |
dbSNP (classic) | rs4699052 |
ClinGen | rs4699052 |
ebi | rs4699052 |
HLI | rs4699052 |
Exac | rs4699052 |
Gnomad | rs4699052 |
Varsome | rs4699052 |
LitVar | rs4699052 |
Map | rs4699052 |
PheGenI | rs4699052 |
Biobank | rs4699052 |
1000 genomes | rs4699052 |
hgdp | rs4699052 |
ensembl | rs4699052 |
geneview | rs4699052 |
scholar | rs4699052 |
rs4699052 | |
pharmgkb | rs4699052 |
gwascentral | rs4699052 |
openSNP | rs4699052 |
23andMe | rs4699052 |
SNPshot | rs4699052 |
SNPdbe | rs4699052 |
MSV3d | rs4699052 |
GWAS Ctlg | rs4699052 |
GMAF | 0.4279 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19483681] |
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] |