rs16859517
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs16859517(C;T) |
Make rs16859517(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 219084462 |
Gene | NHEJ1 |
is a | snp |
is | mentioned by |
dbSNP | rs16859517 |
dbSNP (classic) | rs16859517 |
ClinGen | rs16859517 |
ebi | rs16859517 |
HLI | rs16859517 |
Exac | rs16859517 |
Gnomad | rs16859517 |
Varsome | rs16859517 |
LitVar | rs16859517 |
Map | rs16859517 |
PheGenI | rs16859517 |
Biobank | rs16859517 |
1000 genomes | rs16859517 |
hgdp | rs16859517 |
ensembl | rs16859517 |
geneview | rs16859517 |
scholar | rs16859517 |
rs16859517 | |
pharmgkb | rs16859517 |
gwascentral | rs16859517 |
openSNP | rs16859517 |
23andMe | rs16859517 |
SNPshot | rs16859517 |
SNPdbe | rs16859517 |
MSV3d | rs16859517 |
GWAS Ctlg | rs16859517 |
GMAF | 0.1653 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.
GWAS snp | |
---|---|
PMID | [PMID 20189936] |
Trait | Height |
Title | A genome-wide association study in 19,633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci |
Risk Allele | T |
P-val | 0.000005 |
Odds Ratio | 0.05 [0.03-0.07] cm increase |