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rs4896582

From SNPedia

Orientationplus
Stabilizedplus
Make rs4896582(A;A)
Make rs4896582(A;G)
Make rs4896582(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position142382740
GeneGPR126
is asnp
is mentioned by
dbSNPrs4896582
ebirs4896582
HLIrs4896582
Exacrs4896582
Varsomers4896582
Maprs4896582
PheGenIrs4896582
hapmaprs4896582
1000 genomesrs4896582
hgdprs4896582
ensemblrs4896582
gopubmedrs4896582
geneviewrs4896582
scholarrs4896582
googlers4896582
pharmgkbrs4896582
gwascentralrs4896582
openSNPrs4896582
23andMers4896582
23andMe allrs4896582
SNP Nexus

SNPshotrs4896582
SNPdbers4896582
MSV3drs4896582
GWAS Ctlgrs4896582
GMAF0.4027
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs4896582
PubMedID [PMID 18391950OA-icon.png]
Condition Height
Gene GPR126
Risk Allele A
pValue 2.00E-018
OR 0.38
95% CI 0.28-0.48) cm shorte


OMIM606255
DescSTATURE AS A QUANTITATIVE TRAIT
Variant
Relatedalso
[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


GET Evidence
rs4896582
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary