rs6959212
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6959212(C;C) |
Make rs6959212(C;T) |
Make rs6959212(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 38088724 |
is a | snp |
is | mentioned by |
dbSNP | rs6959212 |
dbSNP (classic) | rs6959212 |
ClinGen | rs6959212 |
ebi | rs6959212 |
HLI | rs6959212 |
Exac | rs6959212 |
Gnomad | rs6959212 |
Varsome | rs6959212 |
LitVar | rs6959212 |
Map | rs6959212 |
PheGenI | rs6959212 |
Biobank | rs6959212 |
1000 genomes | rs6959212 |
hgdp | rs6959212 |
ensembl | rs6959212 |
geneview | rs6959212 |
scholar | rs6959212 |
rs6959212 | |
pharmgkb | rs6959212 |
gwascentral | rs6959212 |
openSNP | rs6959212 |
23andMe | rs6959212 |
SNPshot | rs6959212 |
SNPdbe | rs6959212 |
MSV3d | rs6959212 |
GWAS Ctlg | rs6959212 |
GMAF | 0.3517 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22504420![]() |
Trait | |
Title | Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. |
Risk Allele | T |
P-val | 4E-38 |
Odds Ratio | 0.0700 None |
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-9 |
Odds Ratio | .02 [NR] unit decrease |