rs7971536
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7971536(A;A) |
Make rs7971536(A;T) |
Make rs7971536(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 101980010 |
is a | snp |
is | mentioned by |
dbSNP | rs7971536 |
dbSNP (classic) | rs7971536 |
ClinGen | rs7971536 |
ebi | rs7971536 |
HLI | rs7971536 |
Exac | rs7971536 |
Gnomad | rs7971536 |
Varsome | rs7971536 |
LitVar | rs7971536 |
Map | rs7971536 |
PheGenI | rs7971536 |
Biobank | rs7971536 |
1000 genomes | rs7971536 |
hgdp | rs7971536 |
ensembl | rs7971536 |
geneview | rs7971536 |
scholar | rs7971536 |
rs7971536 | |
pharmgkb | rs7971536 |
gwascentral | rs7971536 |
openSNP | rs7971536 |
23andMe | rs7971536 |
SNPshot | rs7971536 |
SNPdbe | rs7971536 |
MSV3d | rs7971536 |
GWAS Ctlg | rs7971536 |
GMAF | 0.4004 |
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 | 8E-14 |
Odds Ratio | 0.03 [NR] unit decrease |