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rs638882

From SNPedia

Orientationminus
Stabilizedminus
Make rs638882(A;A)
Make rs638882(A;G)
Make rs638882(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position115893327
is asnp
is mentioned by
dbSNPrs638882
ebirs638882
HLIrs638882
Exacrs638882
Varsomers638882
Maprs638882
PheGenIrs638882
hapmaprs638882
1000 genomesrs638882
hgdprs638882
ensemblrs638882
gopubmedrs638882
geneviewrs638882
scholarrs638882
googlers638882
pharmgkbrs638882
gwascentralrs638882
openSNPrs638882
23andMers638882
23andMe allrs638882
SNP Nexus

SNPshotrs638882
SNPdbers638882
MSV3drs638882
GWAS Ctlgrs638882
GMAF0.4747
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 0.0000039999999999999998
Odds Ratio NR NR


GET Evidence
rs638882
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary