rs1052483
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1052483(A;A) |
Make rs1052483(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219069626 |
is a | snp |
is | mentioned by |
dbSNP | rs1052483 |
dbSNP (classic) | rs1052483 |
ClinGen | rs1052483 |
ebi | rs1052483 |
HLI | rs1052483 |
Exac | rs1052483 |
Gnomad | rs1052483 |
Varsome | rs1052483 |
LitVar | rs1052483 |
Map | rs1052483 |
PheGenI | rs1052483 |
Biobank | rs1052483 |
1000 genomes | rs1052483 |
hgdp | rs1052483 |
ensembl | rs1052483 |
geneview | rs1052483 |
scholar | rs1052483 |
rs1052483 | |
pharmgkb | rs1052483 |
gwascentral | rs1052483 |
openSNP | rs1052483 |
23andMe | rs1052483 |
SNPshot | rs1052483 |
SNPdbe | rs1052483 |
MSV3d | rs1052483 |
GWAS Ctlg | rs1052483 |
GMAF | 0.1286 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18391951] |
Trait | Height |
Title | Many sequence variants affecting diversity of adult human height |
Risk Allele | C |
P-val | 9.9999999999999995E-7 |
Odds Ratio | 6.90 [4.16-9.64] % SD taller |
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.