rs6892884
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6892884(C;C) |
Make rs6892884(C;T) |
Make rs6892884(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 171588619 |
is a | snp |
is | mentioned by |
dbSNP | rs6892884 |
dbSNP (classic) | rs6892884 |
ClinGen | rs6892884 |
ebi | rs6892884 |
HLI | rs6892884 |
Exac | rs6892884 |
Gnomad | rs6892884 |
Varsome | rs6892884 |
LitVar | rs6892884 |
Map | rs6892884 |
PheGenI | rs6892884 |
Biobank | rs6892884 |
1000 genomes | rs6892884 |
hgdp | rs6892884 |
ensembl | rs6892884 |
geneview | rs6892884 |
scholar | rs6892884 |
rs6892884 | |
pharmgkb | rs6892884 |
gwascentral | rs6892884 |
openSNP | rs6892884 |
23andMe | rs6892884 |
SNPshot | rs6892884 |
SNPdbe | rs6892884 |
MSV3d | rs6892884 |
GWAS Ctlg | rs6892884 |
GMAF | 0.2851 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960![]() |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | |
P-val | 4E-8 |
Odds Ratio | NR NR |