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rs11645938

From SNPedia

Orientationplus
Stabilizedplus
Make rs11645938(C;C)
Make rs11645938(C;T)
Make rs11645938(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position86791556
is asnp
is mentioned by
dbSNPrs11645938
ebirs11645938
HLIrs11645938
Exacrs11645938
Varsomers11645938
Maprs11645938
PheGenIrs11645938
hapmaprs11645938
1000 genomesrs11645938
hgdprs11645938
ensemblrs11645938
gopubmedrs11645938
geneviewrs11645938
scholarrs11645938
googlers11645938
pharmgkbrs11645938
gwascentralrs11645938
openSNPrs11645938
23andMers11645938
23andMe allrs11645938
SNP Nexus

SNPshotrs11645938
SNPdbers11645938
MSV3drs11645938
GWAS Ctlgrs11645938
GMAF0.03857
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24516880OA-icon.png] Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus

[PMID 24513584] Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition