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rs4910742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs4910742(A;G)
Make rs4910742(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5285279
is asnp
is mentioned by
dbSNPrs4910742
ebirs4910742
HLIrs4910742
Exacrs4910742
Varsomers4910742
Maprs4910742
PheGenIrs4910742
hapmaprs4910742
1000 genomesrs4910742
hgdprs4910742
ensemblrs4910742
gopubmedrs4910742
geneviewrs4910742
scholarrs4910742
googlers4910742
pharmgkbrs4910742
gwascentralrs4910742
openSNPrs4910742
23andMers4910742
23andMe allrs4910742
SNP Nexus

SNPshotrs4910742
SNPdbers4910742
MSV3drs4910742
GWAS Ctlgrs4910742
GMAF0.04775
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs4910742
PubMedID [PMID 18245381OA-icon.png]
Condition Fetal hemoglobin levels
Gene HBB
Risk Allele A
pValue 1.00E-021
OR 0.58
95% CI NR) SD decrease in Hb



GWAS snp
PMID [PMID 22291609OA-icon.png]
Trait
Title A genome-wide association scan on the levels of markers of inflammation in sardinians reveals associations that underpin its complex regulation.
Risk Allele G
P-val 2E-9
Odds Ratio None None


GET Evidence
rs4910742
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.929688
summary



[PMID 23092954OA-icon.png] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.