rs4601530
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4601530(C;C) |
Make rs4601530(C;T) |
Make rs4601530(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 24717620 |
is a | snp |
is | mentioned by |
dbSNP | rs4601530 |
dbSNP (classic) | rs4601530 |
ClinGen | rs4601530 |
ebi | rs4601530 |
HLI | rs4601530 |
Exac | rs4601530 |
Gnomad | rs4601530 |
Varsome | rs4601530 |
LitVar | rs4601530 |
Map | rs4601530 |
PheGenI | rs4601530 |
Biobank | rs4601530 |
1000 genomes | rs4601530 |
hgdp | rs4601530 |
ensembl | rs4601530 |
geneview | rs4601530 |
scholar | rs4601530 |
rs4601530 | |
pharmgkb | rs4601530 |
gwascentral | rs4601530 |
openSNP | rs4601530 |
23andMe | rs4601530 |
SNPshot | rs4601530 |
SNPdbe | rs4601530 |
MSV3d | rs4601530 |
GWAS Ctlg | rs4601530 |
GMAF | 0.3613 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960![]() |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 2E-12 |
Odds Ratio | 0.0300 [NR] meters decrease |