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rs2710057

From SNPedia

Orientationplus
Stabilizedplus
Make rs2710057(G;G)
Make rs2710057(G;T)
Make rs2710057(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position86937000
is asnp
is mentioned by
dbSNPrs2710057
ebirs2710057
HLIrs2710057
Exacrs2710057
Varsomers2710057
Maprs2710057
PheGenIrs2710057
hapmaprs2710057
1000 genomesrs2710057
hgdprs2710057
ensemblrs2710057
gopubmedrs2710057
geneviewrs2710057
scholarrs2710057
googlers2710057
pharmgkbrs2710057
gwascentralrs2710057
openSNPrs2710057
23andMers2710057
23andMe allrs2710057
SNP Nexus

SNPshotrs2710057
SNPdbers2710057
MSV3drs2710057
GWAS Ctlgrs2710057
GMAF0.2304
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19079262]
Trait Bone mineral density (hip)
Title New sequence variants associated with bone mineral density
Risk Allele T
P-val 0.000001
Odds Ratio 0.07 [0.04-0.09] SD decrease



GET Evidence
rs2710057
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.728261
summary