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rs4794665

From SNPedia

Orientationplus
Stabilizedplus
Make rs4794665(A;A)
Make rs4794665(A;G)
Make rs4794665(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position56772968
is asnp
is mentioned by
dbSNPrs4794665
ebirs4794665
HLIrs4794665
Exacrs4794665
Varsomers4794665
Maprs4794665
PheGenIrs4794665
hapmaprs4794665
1000 genomesrs4794665
hgdprs4794665
ensemblrs4794665
gopubmedrs4794665
geneviewrs4794665
scholarrs4794665
googlers4794665
pharmgkbrs4794665
gwascentralrs4794665
openSNPrs4794665
23andMers4794665
23andMe allrs4794665
SNP Nexus

SNPshotrs4794665
SNPdbers4794665
MSV3drs4794665
GWAS Ctlgrs4794665
GMAF0.4353
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele A
P-val 9.9999999999999995E-8
Odds Ratio 3.60 [2.23-4.97] % SD taller


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


[PMID 19197348OA-icon.png] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.


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


[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs4794665
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.492188
summary