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rs383362

From SNPedia

Orientationplus
Stabilizedplus
Make rs383362(G;G)
Make rs383362(G;T)
Make rs383362(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position79211923
GeneWWOX
is asnp
is mentioned by
dbSNPrs383362
ebirs383362
HLIrs383362
Exacrs383362
Varsomers383362
Maprs383362
PheGenIrs383362
hapmaprs383362
1000 genomesrs383362
hgdprs383362
ensemblrs383362
gopubmedrs383362
geneviewrs383362
scholarrs383362
googlers383362
pharmgkbrs383362
gwascentralrs383362
openSNPrs383362
23andMers383362
23andMe allrs383362
SNP Nexus

SNPshotrs383362
SNPdbers383362
MSV3drs383362
GWAS Ctlgrs383362
GMAF0.3508
Max Magnitude
? (G;G) (G;T) (T;T) 28
Venter snp
Source plos
Gene Q9NZC7-8
allele T
frequency 0.583
sift TOLERATED
HuRef 1103645525015
Disease Association Defects in WWOX may be involved in esophageal squamous cell carcinoma (ESCC) (MIM:133239).



Neighborrs2288034
Distance136


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


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


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