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rs1126179

From SNPedia

Orientationminus
Stabilizedminus
Make rs1126179(C;C)
Make rs1126179(C;T)
Make rs1126179(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position65861461
GeneLOC101927676
is asnp
is mentioned by
dbSNPrs1126179
ebirs1126179
HLIrs1126179
Exacrs1126179
Varsomers1126179
Maprs1126179
PheGenIrs1126179
hapmaprs1126179
1000 genomesrs1126179
hgdprs1126179
ensemblrs1126179
gopubmedrs1126179
geneviewrs1126179
scholarrs1126179
googlers1126179
pharmgkbrs1126179
gwascentralrs1126179
openSNPrs1126179
23andMers1126179
23andMe allrs1126179
SNP Nexus

SNPshotrs1126179
SNPdbers1126179
MSV3drs1126179
GWAS Ctlgrs1126179
GMAF0.3641
Max Magnitude
? (C;C) (C;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 G
P-val 3E-6
Odds Ratio 2.13 [1.55-2.92]