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rs4811117

From SNPedia

Orientationplus
Stabilizedplus
Make rs4811117(G;G)
Make rs4811117(G;T)
Make rs4811117(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position51054898
is asnp
is mentioned by
dbSNPrs4811117
ebirs4811117
HLIrs4811117
Exacrs4811117
Varsomers4811117
Maprs4811117
PheGenIrs4811117
hapmaprs4811117
1000 genomesrs4811117
hgdprs4811117
ensemblrs4811117
gopubmedrs4811117
geneviewrs4811117
scholarrs4811117
googlers4811117
pharmgkbrs4811117
gwascentralrs4811117
openSNPrs4811117
23andMers4811117
23andMe allrs4811117
SNP Nexus

SNPshotrs4811117
SNPdbers4811117
MSV3drs4811117
GWAS Ctlgrs4811117
GMAF0.1428
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23918034]
Trait Molar-incisor hypomineralization
Title Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).
Risk Allele T
P-val 5E-6
Odds Ratio 3.13 [1.92-5.13]