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rs4549631

From SNPedia

Orientationplus
Stabilizedplus
Make rs4549631(C;C)
Make rs4549631(C;T)
Make rs4549631(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position126645162
GeneLOC728666
is asnp
is mentioned by
dbSNPrs4549631
dbSNP (classic)rs4549631
ClinGenrs4549631
ebirs4549631
HLIrs4549631
Exacrs4549631
Gnomadrs4549631
Varsomers4549631
LitVarrs4549631
Maprs4549631
PheGenIrs4549631
Biobankrs4549631
1000 genomesrs4549631
hgdprs4549631
ensemblrs4549631
geneviewrs4549631
scholarrs4549631
googlers4549631
pharmgkbrs4549631
gwascentralrs4549631
openSNPrs4549631
23andMers4549631
SNPshotrs4549631
SNPdbers4549631
MSV3drs4549631
GWAS Ctlgrs4549631
GMAF0.3944
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele C
P-val 4.9999999999999999E-13
Odds Ratio 0.06 [0.03-0.08] SD taller - among males


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.