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rs11692564

From SNPedia

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Make rs11692564(C;C)
Make rs11692564(C;T)
Make rs11692564(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position118788418
is asnp
is mentioned by
dbSNPrs11692564
ebirs11692564
HLIrs11692564
Exacrs11692564
Varsomers11692564
Maprs11692564
PheGenIrs11692564
hapmaprs11692564
1000 genomesrs11692564
hgdprs11692564
ensemblrs11692564
gopubmedrs11692564
geneviewrs11692564
scholarrs11692564
googlers11692564
pharmgkbrs11692564
gwascentralrs11692564
openSNPrs11692564
23andMers11692564
23andMe allrs11692564
SNP Nexus

SNPshotrs11692564
SNPdbers11692564
MSV3drs11692564
GWAS Ctlgrs11692564
Max Magnitude
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.