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rs2814828

From SNPedia

Orientationplus
Stabilizedplus
Make rs2814828(C;C)
Make rs2814828(C;T)
Make rs2814828(T;T)
ReferenceGRCh37 37.1/131
Chromosome9
Position90811182
GeneLOC100129340
is asnp
is mentioned by
dbSNPrs2814828
ebirs2814828
HLIrs2814828
Exacrs2814828
Varsomers2814828
Maprs2814828
PheGenIrs2814828
hapmaprs2814828
1000 genomesrs2814828
hgdprs2814828
ensemblrs2814828
gopubmedrs2814828
geneviewrs2814828
scholarrs2814828
googlers2814828
pharmgkbrs2814828
gwascentralrs2814828
openSNPrs2814828
23andMers2814828
23andMe allrs2814828
SNP Nexus

SNPshotrs2814828
SNPdbers2814828
MSV3drs2814828
GWAS Ctlgrs2814828
GMAF0.3655
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele T
P-val 8.9999999999999996E-7
Odds Ratio 5.40 [3.24-7.56] % SD taller


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


GET Evidence
rs2814828
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.695312
summary