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rs1239947

From SNPedia

Orientationminus
Stabilizedplus
Make rs1239947(A;A)
Make rs1239947(A;G)
Make rs1239947(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position50532419
is asnp
is mentioned by
dbSNPrs1239947
ebirs1239947
HLIrs1239947
Exacrs1239947
Varsomers1239947
Maprs1239947
PheGenIrs1239947
hapmaprs1239947
1000 genomesrs1239947
hgdprs1239947
ensemblrs1239947
gopubmedrs1239947
geneviewrs1239947
scholarrs1239947
googlers1239947
pharmgkbrs1239947
gwascentralrs1239947
openSNPrs1239947
23andMers1239947
23andMe allrs1239947
SNP Nexus

SNPshotrs1239947
SNPdbers1239947
MSV3drs1239947
GWAS Ctlgrs1239947
GMAF0.2548
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 G
P-val 0.0000079999999999999996
Odds Ratio 3.80 [2.23-5.37] % SD taller

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


GET Evidence
rs1239947
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.695312
summary