rs6724465
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs6724465(A;A) |
Make rs6724465(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219079124 |
Gene | NHEJ1 |
is a | snp |
is | mentioned by |
dbSNP | rs6724465 |
dbSNP (classic) | rs6724465 |
ClinGen | rs6724465 |
ebi | rs6724465 |
HLI | rs6724465 |
Exac | rs6724465 |
Gnomad | rs6724465 |
Varsome | rs6724465 |
LitVar | rs6724465 |
Map | rs6724465 |
PheGenI | rs6724465 |
Biobank | rs6724465 |
1000 genomes | rs6724465 |
hgdp | rs6724465 |
ensembl | rs6724465 |
geneview | rs6724465 |
scholar | rs6724465 |
rs6724465 | |
pharmgkb | rs6724465 |
gwascentral | rs6724465 |
openSNP | rs6724465 |
23andMe | rs6724465 |
SNPshot | rs6724465 |
SNPdbe | rs6724465 |
MSV3d | rs6724465 |
GWAS Ctlg | rs6724465 |
GMAF | 0.1111 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18391952] |
Trait | Height |
Title | Genome-wide association analysis identifies 20 loci that influence adult height |
Risk Allele | A |
P-val | 2E-8 |
Odds Ratio | 0.06 [0.02-0.10] SD shorter - among males |
[PMID 19030899] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
[PMID 19039035] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
[PMID 19481195] The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
[PMID 20017971] Assessing the impact of global versus local ancestry in association studies.