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rs3006564

From SNPedia

Orientationplus
Stabilizedplus
Make rs3006564(C;C)
Make rs3006564(C;T)
Make rs3006564(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position29888959
is asnp
is mentioned by
dbSNPrs3006564
ebirs3006564
HLIrs3006564
Exacrs3006564
Varsomers3006564
Maprs3006564
PheGenIrs3006564
hapmaprs3006564
1000 genomesrs3006564
hgdprs3006564
ensemblrs3006564
gopubmedrs3006564
geneviewrs3006564
scholarrs3006564
googlers3006564
pharmgkbrs3006564
gwascentralrs3006564
openSNPrs3006564
23andMers3006564
23andMe allrs3006564
SNP Nexus

SNPshotrs3006564
SNPdbers3006564
MSV3drs3006564
GWAS Ctlgrs3006564
GMAF0.4376
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22419666OA-icon.png]
Trait
Title Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
Risk Allele
P-val 0.000005
Odds Ratio 1.3200 None