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rs4954956

From SNPedia

Orientationplus
Stabilizedplus
Make rs4954956(C;C)
Make rs4954956(C;T)
Make rs4954956(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position138787007
GeneNXPH2
is asnp
is mentioned by
dbSNPrs4954956
ebirs4954956
HLIrs4954956
Exacrs4954956
Varsomers4954956
Maprs4954956
PheGenIrs4954956
hapmaprs4954956
1000 genomesrs4954956
hgdprs4954956
ensemblrs4954956
gopubmedrs4954956
geneviewrs4954956
scholarrs4954956
googlers4954956
pharmgkbrs4954956
gwascentralrs4954956
openSNPrs4954956
23andMers4954956
23andMe allrs4954956
SNP Nexus

SNPshotrs4954956
SNPdbers4954956
MSV3drs4954956
GWAS Ctlgrs4954956
GMAF0.2668
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19304784OA-icon.png] 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.
OMIM167000
Desc
Variant
Relatedalso