rs4954956
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4954956(C;C) |
Make rs4954956(C;T) |
Make rs4954956(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 138787007 |
Gene | NXPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs4954956 |
dbSNP (classic) | rs4954956 |
ClinGen | rs4954956 |
ebi | rs4954956 |
HLI | rs4954956 |
Exac | rs4954956 |
Gnomad | rs4954956 |
Varsome | rs4954956 |
LitVar | rs4954956 |
Map | rs4954956 |
PheGenI | rs4954956 |
Biobank | rs4954956 |
1000 genomes | rs4954956 |
hgdp | rs4954956 |
ensembl | rs4954956 |
geneview | rs4954956 |
scholar | rs4954956 |
rs4954956 | |
pharmgkb | rs4954956 |
gwascentral | rs4954956 |
openSNP | rs4954956 |
23andMe | rs4954956 |
SNPshot | rs4954956 |
SNPdbe | rs4954956 |
MSV3d | rs4954956 |
GWAS Ctlg | rs4954956 |
GMAF | 0.2668 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19304784] rs4954956 was associated with increased ovarian cancer risk, particularly for serous ovarian cancer. The per minor allele odds ratio was 1.07 (CI: 1.01-1.13, P-trend=0.02) for all types of ovarian cancer and 1.14 (CI: 1.07-1.22, P-trend=0.00017) for serous ovarian cancer in this study of 2927 invasive ovarian cancer cases and 4143 controls from six ovarian cancer case-control studies.