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rs2054989

From SNPedia

Orientationplus
Stabilizedplus
Make rs2054989(A;A)
Make rs2054989(A;G)
Make rs2054989(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position56496681
is asnp
is mentioned by
dbSNPrs2054989
ebirs2054989
HLIrs2054989
Exacrs2054989
Varsomers2054989
Maprs2054989
PheGenIrs2054989
hapmaprs2054989
1000 genomesrs2054989
hgdprs2054989
ensemblrs2054989
gopubmedrs2054989
geneviewrs2054989
scholarrs2054989
googlers2054989
pharmgkbrs2054989
gwascentralrs2054989
openSNPrs2054989
23andMers2054989
23andMe allrs2054989
SNP Nexus

SNPshotrs2054989
SNPdbers2054989
MSV3drs2054989
GWAS Ctlgrs2054989
GMAF0.3627
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Hip geometry
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 5.9999999999999997E-7
Odds Ratio NR NR


GET Evidence
rs2054989
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.671875
summary