Have questions? Visit https://www.reddit.com/r/SNPedia

rs16864755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16864755(A;A)
Make rs16864755(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position223409904
GeneLOC100289013
is asnp
is mentioned by
dbSNPrs16864755
ebirs16864755
HLIrs16864755
Exacrs16864755
Varsomers16864755
Maprs16864755
PheGenIrs16864755
hapmaprs16864755
1000 genomesrs16864755
hgdprs16864755
ensemblrs16864755
gopubmedrs16864755
geneviewrs16864755
scholarrs16864755
googlers16864755
pharmgkbrs16864755
gwascentralrs16864755
openSNPrs16864755
23andMers16864755
23andMe allrs16864755
SNP Nexus

SNPshotrs16864755
SNPdbers16864755
MSV3drs16864755
GWAS Ctlgrs16864755
GMAF0.05005
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20200953OA-icon.png]
Trait Osteoporosis-related phenotypes
Title Genome-wide pleiotropy of osteoporosis-related phenotypes: The Framingham study.
Risk Allele
P-val 0.000004
Odds Ratio 0.24 [0.14-0.34] cm3 increase