rs4896582
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4896582(A;A) |
Make rs4896582(A;G) |
Make rs4896582(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 142382740 |
Gene | ADGRG6 |
is a | snp |
is | mentioned by |
dbSNP | rs4896582 |
dbSNP (classic) | rs4896582 |
ClinGen | rs4896582 |
ebi | rs4896582 |
HLI | rs4896582 |
Exac | rs4896582 |
Gnomad | rs4896582 |
Varsome | rs4896582 |
LitVar | rs4896582 |
Map | rs4896582 |
PheGenI | rs4896582 |
Biobank | rs4896582 |
1000 genomes | rs4896582 |
hgdp | rs4896582 |
ensembl | rs4896582 |
geneview | rs4896582 |
scholar | rs4896582 |
rs4896582 | |
pharmgkb | rs4896582 |
gwascentral | rs4896582 |
openSNP | rs4896582 |
23andMe | rs4896582 |
SNPshot | rs4896582 |
SNPdbe | rs4896582 |
MSV3d | rs4896582 |
GWAS Ctlg | rs4896582 |
GMAF | 0.4027 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs4896582 |
PubMedID | [PMID 18391950] |
Condition | Height |
Gene | GPR126 |
Risk Allele | A |
pValue | 2.00E-018 |
OR | 0.38 |
95% CI | 0.28-0.48) cm shorte |
[PMID 19030899] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.