Have questions? Visit https://www.reddit.com/r/SNPedia

rs11228719

From SNPedia

Orientationplus
Stabilizedplus
Make rs11228719(C;C)
Make rs11228719(C;T)
Make rs11228719(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position56672760
is asnp
is mentioned by
dbSNPrs11228719
ebirs11228719
HLIrs11228719
Exacrs11228719
Varsomers11228719
Maprs11228719
PheGenIrs11228719
hapmaprs11228719
1000 genomesrs11228719
hgdprs11228719
ensemblrs11228719
gopubmedrs11228719
geneviewrs11228719
scholarrs11228719
googlers11228719
pharmgkbrs11228719
gwascentralrs11228719
openSNPrs11228719
23andMers11228719
23andMe allrs11228719
SNP Nexus

SNPshotrs11228719
SNPdbers11228719
MSV3drs11228719
GWAS Ctlgrs11228719
GMAF0.377
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 0.000004
Odds Ratio 1.6400 None