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rs1074963

From SNPedia

Orientationplus
Make rs1074963(C;C)
Make rs1074963(C;G)
Make rs1074963(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position78136263
GeneWWOX
is asnp
is mentioned by
dbSNPrs1074963
ebirs1074963
HLIrs1074963
Exacrs1074963
Varsomers1074963
Maprs1074963
PheGenIrs1074963
hapmaprs1074963
1000 genomesrs1074963
hgdprs1074963
ensemblrs1074963
gopubmedrs1074963
geneviewrs1074963
scholarrs1074963
googlers1074963
pharmgkbrs1074963
gwascentralrs1074963
openSNPrs1074963
23andMers1074963
23andMe allrs1074963
SNP Nexus

SNPshotrs1074963
SNPdbers1074963
MSV3drs1074963
GWAS Ctlgrs1074963
Max Magnitude
? (C;C) (C;G) (G;G) 28

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