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rs4916483

From SNPedia

Orientationminus
Stabilizedminus
Make rs4916483(A;A)
Make rs4916483(A;G)
Make rs4916483(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position196180782
is asnp
is mentioned by
dbSNPrs4916483
ebirs4916483
HLIrs4916483
Exacrs4916483
Varsomers4916483
Maprs4916483
PheGenIrs4916483
hapmaprs4916483
1000 genomesrs4916483
hgdprs4916483
ensemblrs4916483
gopubmedrs4916483
geneviewrs4916483
scholarrs4916483
googlers4916483
pharmgkbrs4916483
gwascentralrs4916483
openSNPrs4916483
23andMers4916483
23andMe allrs4916483
SNP Nexus

SNPshotrs4916483
SNPdbers4916483
MSV3drs4916483
GWAS Ctlgrs4916483
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20139978]
Trait Mean corpuscular hemoglobin
Title Genome-wide association study of hematological and biochemical traits in a Japanese population.
Risk Allele C
P-val 4E-11
Odds Ratio .08 [0.054-0.102] unit decrease