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rs877776

From SNPedia

Orientationminus
Stabilizedminus
Make rs877776(C;C)
Make rs877776(C;G)
Make rs877776(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position152205542
GeneOR4R2P
is asnp
is mentioned by
dbSNPrs877776
ebirs877776
HLIrs877776
Exacrs877776
Varsomers877776
Maprs877776
PheGenIrs877776
hapmaprs877776
1000 genomesrs877776
hgdprs877776
ensemblrs877776
gopubmedrs877776
geneviewrs877776
scholarrs877776
googlers877776
pharmgkbrs877776
gwascentralrs877776
openSNPrs877776
23andMers877776
23andMe allrs877776
SNP Nexus

SNPshotrs877776
SNPdbers877776
MSV3drs877776
GWAS Ctlgrs877776
GMAF0.3972
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20109745OA-icon.png] Chromosome 11q13.5 variant associated with childhood eczema: An effect supplementary to filaggrin mutations


[PMID 23557745] Association of the chromosome 11q13.5 variant with atopic dermatitis in Austrian patients