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rs2288033

From SNPedia

Orientationminus
Stabilizedminus
Make rs2288033(A;A)
Make rs2288033(A;G)
Make rs2288033(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position79212064
GeneWWOX
is asnp
is mentioned by
dbSNPrs2288033
ebirs2288033
HLIrs2288033
Exacrs2288033
Varsomers2288033
Maprs2288033
PheGenIrs2288033
hapmaprs2288033
1000 genomesrs2288033
hgdprs2288033
ensemblrs2288033
gopubmedrs2288033
geneviewrs2288033
scholarrs2288033
googlers2288033
pharmgkbrs2288033
gwascentralrs2288033
openSNPrs2288033
23andMers2288033
23andMe allrs2288033
SNP Nexus

SNPshotrs2288033
SNPdbers2288033
MSV3drs2288033
GWAS Ctlgrs2288033
GMAF0.4702
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene Q9NZC7-8
allele C
frequency 0.673
sift TOLERATED
HuRef 1103645525017
Disease Association Defects in WWOX may be involved in esophageal squamous cell carcinoma (ESCC) (MIM:133239).



Neighborrs2288034
Distance5