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rs749052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs749052(A;G)
Make rs749052(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position231931900
is asnp
is mentioned by
dbSNPrs749052
ebirs749052
HLIrs749052
Exacrs749052
Varsomers749052
Maprs749052
PheGenIrs749052
hapmaprs749052
1000 genomesrs749052
hgdprs749052
ensemblrs749052
gopubmedrs749052
geneviewrs749052
scholarrs749052
googlers749052
pharmgkbrs749052
gwascentralrs749052
openSNPrs749052
23andMers749052
23andMe allrs749052
SNP Nexus

SNPshotrs749052
SNPdbers749052
MSV3drs749052
GWAS Ctlgrs749052
GMAF0.05923
Max Magnitude0
? (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-7
Odds Ratio 8.70 [5.17-12.23] % SD taller

[PMID 18471798OA-icon.png] Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.

[PMID 19570815OA-icon.png] A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.

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


GET Evidence
rs749052
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary