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rs2165468

From SNPedia

Orientationminus
Stabilizedminus
Make rs2165468(G;G)
Make rs2165468(G;T)
Make rs2165468(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position3473913
is asnp
is mentioned by
dbSNPrs2165468
ClinGenrs2165468
ebirs2165468
HLIrs2165468
Exacrs2165468
Varsomers2165468
Maprs2165468
PheGenIrs2165468
hapmaprs2165468
1000 genomesrs2165468
hgdprs2165468
ensemblrs2165468
gopubmedrs2165468
geneviewrs2165468
scholarrs2165468
googlers2165468
pharmgkbrs2165468
gwascentralrs2165468
openSNPrs2165468
23andMers2165468
23andMe allrs2165468
SNP Nexus

SNPshotrs2165468
SNPdbers2165468
MSV3drs2165468
GWAS Ctlgrs2165468
GMAF0.2883
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Bone mineral density
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR


GET Evidence
rs2165468
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.253968
summary