rs11692564
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs11692564(C;T) |
Make rs11692564(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 118788418 |
is a | snp |
is | mentioned by |
dbSNP | rs11692564 |
dbSNP (classic) | rs11692564 |
ClinGen | rs11692564 |
ebi | rs11692564 |
HLI | rs11692564 |
Exac | rs11692564 |
Gnomad | rs11692564 |
Varsome | rs11692564 |
LitVar | rs11692564 |
Map | rs11692564 |
PheGenI | rs11692564 |
Biobank | rs11692564 |
1000 genomes | rs11692564 |
hgdp | rs11692564 |
ensembl | rs11692564 |
geneview | rs11692564 |
scholar | rs11692564 |
rs11692564 | |
pharmgkb | rs11692564 |
gwascentral | rs11692564 |
openSNP | rs11692564 |
23andMe | rs11692564 |
SNPshot | rs11692564 |
SNPdbe | rs11692564 |
MSV3d | rs11692564 |
GWAS Ctlg | rs11692564 |
Max Magnitude | 0 |
10.1038/nature14878 The rs11692564(T) allele, located 53 kilobase pairs (kb) downstream from the engrailed homeobox‐1 EN1 gene on chromosome 2, was found to be associated with an increase in bone density in both replications and meta-analyses, with an average increase of +0.22 s.d. (p = 2x10e-14).
[PMID 26970088] Rare EN1 Variants and Pediatric Bone Mass.