rs26868
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs26868(A;A) |
Make rs26868(A;T) |
Make rs26868(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 2199375 |
is a | snp |
is | mentioned by |
dbSNP | rs26868 |
dbSNP (classic) | rs26868 |
ClinGen | rs26868 |
ebi | rs26868 |
HLI | rs26868 |
Exac | rs26868 |
Gnomad | rs26868 |
Varsome | rs26868 |
LitVar | rs26868 |
Map | rs26868 |
PheGenI | rs26868 |
Biobank | rs26868 |
1000 genomes | rs26868 |
hgdp | rs26868 |
ensembl | rs26868 |
geneview | rs26868 |
scholar | rs26868 |
rs26868 | |
pharmgkb | rs26868 |
gwascentral | rs26868 |
openSNP | rs26868 |
23andMe | rs26868 |
SNPshot | rs26868 |
SNPdbe | rs26868 |
MSV3d | rs26868 |
GWAS Ctlg | rs26868 |
GMAF | 0.3664 |
Max Magnitude | 0 |
? | (A;A) (A;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 | A |
P-val | 9E-17 |
Odds Ratio | 0.03 [NR] unit increase |