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rs3764340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3764340(C;G)
Make rs3764340(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position78432540
GeneWWOX
is asnp
is mentioned by
dbSNPrs3764340
dbSNP (classic)rs3764340
ClinGenrs3764340
ebirs3764340
HLIrs3764340
Exacrs3764340
Gnomadrs3764340
Varsomers3764340
LitVarrs3764340
Maprs3764340
PheGenIrs3764340
Biobankrs3764340
1000 genomesrs3764340
hgdprs3764340
ensemblrs3764340
geneviewrs3764340
scholarrs3764340
googlers3764340
pharmgkbrs3764340
gwascentralrs3764340
openSNPrs3764340
23andMers3764340
SNPshotrs3764340
SNPdbers3764340
MSV3drs3764340
GWAS Ctlgrs3764340
GMAF0.07759
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 23197378] Genetic and epigenetic alterations of WWOX in the development of gastric cardia adenocarcinoma


[PMID 21520031] Evidences that the polymorphism Pro-282-Ala within the tumor suppressor gene WWOX is a new risk factor for differentiated thyroid carcinoma.


[PMID 22213016] Decreased expression of WWOX in the development of esophageal squamous cell carcinoma.


[PMID 22693020] The polymorphisms and haplotypes of WWOX gene are associated with the risk of lung cancer in southern and eastern Chinese populations.


[PMID 26902998OA-icon.png] The role of WWOX polymorphisms on COPD susceptibility and pulmonary function traits in Chinese: a case-control study and family-based analysis.


[PMID 26929649OA-icon.png] Association of polymorphisms in WWOX gene with risk and outcome of osteosarcoma in a sample of the young Chinese population.


ClinVar
Risk rs3764340(G;G)
Alt rs3764340(G;G)
Reference Rs3764340(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene WWOX
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.78466437C>G
CLNSRC
CLNACC RCV000249793.2,



[PMID 30013442OA-icon.png] Relationship of genetic variant distributions of WW domain-containing oxidoreductase gene with uterine cervical cancer.