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rs10490823

From SNPedia

Orientationminus
Stabilizedminus
Make rs10490823(A;A)
Make rs10490823(A;G)
Make rs10490823(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position41082244
is asnp
is mentioned by
dbSNPrs10490823
ebirs10490823
HLIrs10490823
Exacrs10490823
Varsomers10490823
Maprs10490823
PheGenIrs10490823
hapmaprs10490823
1000 genomesrs10490823
hgdprs10490823
ensemblrs10490823
gopubmedrs10490823
geneviewrs10490823
scholarrs10490823
googlers10490823
pharmgkbrs10490823
gwascentralrs10490823
openSNPrs10490823
23andMers10490823
23andMe allrs10490823
SNP Nexus

SNPshotrs10490823
SNPdbers10490823
MSV3drs10490823
GWAS Ctlgrs10490823
GMAF0.3416
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19079262]
Trait Bone mineral density (hip)
Title New sequence variants associated with bone mineral density
Risk Allele G
P-val 0.000009
Odds Ratio 0.06 [0.03-0.09] SD decrease



GET Evidence
rs10490823
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary