rs6457821
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 |
Make rs6457821(A;A) |
Make rs6457821(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 35435028 |
is a | snp |
is | mentioned by |
dbSNP | rs6457821 |
dbSNP (classic) | rs6457821 |
ClinGen | rs6457821 |
ebi | rs6457821 |
HLI | rs6457821 |
Exac | rs6457821 |
Gnomad | rs6457821 |
Varsome | rs6457821 |
LitVar | rs6457821 |
Map | rs6457821 |
PheGenI | rs6457821 |
Biobank | rs6457821 |
1000 genomes | rs6457821 |
hgdp | rs6457821 |
ensembl | rs6457821 |
geneview | rs6457821 |
scholar | rs6457821 |
rs6457821 | |
pharmgkb | rs6457821 |
gwascentral | rs6457821 |
openSNP | rs6457821 |
23andMe | rs6457821 |
SNPshot | rs6457821 |
SNPdbe | rs6457821 |
MSV3d | rs6457821 |
GWAS Ctlg | rs6457821 |
GMAF | 0.02388 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | A |
P-val | 2E-12 |
Odds Ratio | .10 [NR] unit decrease |