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rs6747776

From SNPedia

Orientationplus
Stabilizedplus
Make rs6747776(C;C)
Make rs6747776(C;G)
Make rs6747776(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position218860595
GeneWNT6
is asnp
is mentioned by
dbSNPrs6747776
ebirs6747776
HLIrs6747776
Exacrs6747776
Varsomers6747776
Maprs6747776
PheGenIrs6747776
hapmaprs6747776
1000 genomesrs6747776
hgdprs6747776
ensemblrs6747776
gopubmedrs6747776
geneviewrs6747776
scholarrs6747776
googlers6747776
pharmgkbrs6747776
gwascentralrs6747776
openSNPrs6747776
23andMers6747776
23andMe allrs6747776
SNP Nexus

SNPshotrs6747776
SNPdbers6747776
MSV3drs6747776
GWAS Ctlgrs6747776
GMAF0.3866
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 21547848OA-icon.png] Polymorphisms in WNT6 and WNT10A and Colorectal Adenoma Risk