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rs1021188

From SNPedia

Orientationplus
Stabilizedplus
Make rs1021188(C;C)
Make rs1021188(C;T)
Make rs1021188(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position42541997
is asnp
is mentioned by
dbSNPrs1021188
ebirs1021188
HLIrs1021188
Exacrs1021188
Varsomers1021188
Maprs1021188
PheGenIrs1021188
hapmaprs1021188
1000 genomesrs1021188
hgdprs1021188
ensemblrs1021188
gopubmedrs1021188
geneviewrs1021188
scholarrs1021188
googlers1021188
pharmgkbrs1021188
gwascentralrs1021188
openSNPrs1021188
23andMers1021188
23andMe allrs1021188
SNP Nexus

SNPshotrs1021188
SNPdbers1021188
MSV3drs1021188
GWAS Ctlgrs1021188
GMAF0.2429
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21124946OA-icon.png] Genome-Wide Association Meta-Analysis of Cortical Bone Mineral Density Unravels Allelic Heterogeneity at the RANKL Locus and Potential Pleiotropic Effects on Bone
GWAS snp
PMID [PMID 23437003OA-icon.png]
Trait Bone mineral density
Title Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.
Risk Allele C
P-val 4E-14
Odds Ratio .15 [0.11-0.19] unit decrease


[PMID 25464125] RANK/RANKL/OPG pathway: genetic associations with stress fracture period prevalence in elite athletes