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rs4904868

From SNPedia

Orientationplus
Stabilizedplus
Make rs4904868(C;C)
Make rs4904868(C;T)
Make rs4904868(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position92314657
is asnp
is mentioned by
dbSNPrs4904868
ebirs4904868
HLIrs4904868
Exacrs4904868
Varsomers4904868
Maprs4904868
PheGenIrs4904868
hapmaprs4904868
1000 genomesrs4904868
hgdprs4904868
ensemblrs4904868
gopubmedrs4904868
geneviewrs4904868
scholarrs4904868
googlers4904868
pharmgkbrs4904868
gwascentralrs4904868
openSNPrs4904868
23andMers4904868
23andMe allrs4904868
SNP Nexus

SNPshotrs4904868
SNPdbers4904868
MSV3drs4904868
GWAS Ctlgrs4904868
GMAF0.3811
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs4904868,rs2402130
PubMedID [PMID 17952075]
Condition Blue vs. green eyes
Gene SLC24A4
Risk Allele A
pValue 2.00E-018
OR 2.06
95% CI 1.76-2.42



[PMID 20585627OA-icon.png] Web-based, participant-driven studies yield novel genetic associations for common traits.


GET Evidence
rs4904868
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.398438
summary