rs7697556
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7697556(C;C) |
Make rs7697556(C;T) |
Make rs7697556(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 72649596 |
is a | snp |
is | mentioned by |
dbSNP | rs7697556 |
dbSNP (classic) | rs7697556 |
ClinGen | rs7697556 |
ebi | rs7697556 |
HLI | rs7697556 |
Exac | rs7697556 |
Gnomad | rs7697556 |
Varsome | rs7697556 |
LitVar | rs7697556 |
Map | rs7697556 |
PheGenI | rs7697556 |
Biobank | rs7697556 |
1000 genomes | rs7697556 |
hgdp | rs7697556 |
ensembl | rs7697556 |
geneview | rs7697556 |
scholar | rs7697556 |
rs7697556 | |
pharmgkb | rs7697556 |
gwascentral | rs7697556 |
openSNP | rs7697556 |
23andMe | rs7697556 |
SNPshot | rs7697556 |
SNPdbe | rs7697556 |
MSV3d | rs7697556 |
GWAS Ctlg | rs7697556 |
GMAF | 0.4481 |
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 | T |
P-val | 2E-14 |
Odds Ratio | 0.03 [NR] unit increase |