rs6714546
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6714546(A;A) |
Make rs6714546(A;G) |
Make rs6714546(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 33136358 |
Gene | LTBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs6714546 |
dbSNP (classic) | rs6714546 |
ClinGen | rs6714546 |
ebi | rs6714546 |
HLI | rs6714546 |
Exac | rs6714546 |
Gnomad | rs6714546 |
Varsome | rs6714546 |
LitVar | rs6714546 |
Map | rs6714546 |
PheGenI | rs6714546 |
Biobank | rs6714546 |
1000 genomes | rs6714546 |
hgdp | rs6714546 |
ensembl | rs6714546 |
geneview | rs6714546 |
scholar | rs6714546 |
rs6714546 | |
pharmgkb | rs6714546 |
gwascentral | rs6714546 |
openSNP | rs6714546 |
23andMe | rs6714546 |
SNPshot | rs6714546 |
SNPdbe | rs6714546 |
MSV3d | rs6714546 |
GWAS Ctlg | rs6714546 |
GMAF | 0.1547 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | A |
P-val | 2E-9 |
Odds Ratio | 0.0300 [NR] meters decrease |