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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
ebirs4549631
HLIrs4549631
Exacrs4549631
Varsomers4549631
Maprs4549631
PheGenIrs4549631
hapmaprs4549631
1000 genomesrs4549631
hgdprs4549631
ensemblrs4549631
gopubmedrs4549631
geneviewrs4549631
scholarrs4549631
googlers4549631
pharmgkbrs4549631
gwascentralrs4549631
openSNPrs4549631
23andMers4549631
23andMe allrs4549631
SNP Nexus

SNPshotrs4549631
SNPdbers4549631
MSV3drs4549631
GWAS Ctlgrs4549631
GMAF0.3944
Max Magnitude
? (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.


GET Evidence
rs4549631
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary