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rs2288034

From SNPedia

Orientationminus
Stabilizedminus
Make rs2288034(C;C)
Make rs2288034(C;G)
Make rs2288034(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position79212059
GeneWWOX
is asnp
is mentioned by
dbSNPrs2288034
ebirs2288034
HLIrs2288034
Exacrs2288034
Varsomers2288034
Maprs2288034
PheGenIrs2288034
hapmaprs2288034
1000 genomesrs2288034
hgdprs2288034
ensemblrs2288034
gopubmedrs2288034
geneviewrs2288034
scholarrs2288034
googlers2288034
pharmgkbrs2288034
gwascentralrs2288034
openSNPrs2288034
23andMers2288034
23andMe allrs2288034
SNP Nexus

SNPshotrs2288034
SNPdbers2288034
MSV3drs2288034
GWAS Ctlgrs2288034
GMAF0.4688
Max Magnitude
? (C;C) (C;G) (G;G) 28
Venter snp
Source plos
Gene Q9NZC7-8
allele G
frequency 0.684
sift TOLERATED
HuRef 1103645525016
Disease Association Defects in WWOX may be involved in esophageal squamous cell carcinoma (ESCC) (MIM:133239).



Neighborrs383362
Distance136
Neighborrs2288033
Distance5