rs673604
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs673604(C;C) |
Make rs673604(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 35222214 |
is a | snp |
is | mentioned by |
dbSNP | rs673604 |
dbSNP (classic) | rs673604 |
ClinGen | rs673604 |
ebi | rs673604 |
HLI | rs673604 |
Exac | rs673604 |
Gnomad | rs673604 |
Varsome | rs673604 |
LitVar | rs673604 |
Map | rs673604 |
PheGenI | rs673604 |
Biobank | rs673604 |
1000 genomes | rs673604 |
hgdp | rs673604 |
ensembl | rs673604 |
geneview | rs673604 |
scholar | rs673604 |
rs673604 | |
pharmgkb | rs673604 |
gwascentral | rs673604 |
openSNP | rs673604 |
23andMe | rs673604 |
SNPshot | rs673604 |
SNPdbe | rs673604 |
MSV3d | rs673604 |
GWAS Ctlg | rs673604 |
GMAF | 0.3985 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21499250![]() |
Trait | |
Title | Genome-wide association study identifies a common variant associated with risk of endometrial cancer. |
Risk Allele | |
P-val | 0.000006 |
Odds Ratio | 1.2100 [1.12-1.32] |