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rs1006899

From SNPedia

Orientationplus
Stabilizedplus
Make rs1006899(A;A)
Make rs1006899(A;G)
Make rs1006899(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position14472731
is asnp
is mentioned by
dbSNPrs1006899
ebirs1006899
HLIrs1006899
Exacrs1006899
Varsomers1006899
Maprs1006899
PheGenIrs1006899
hapmaprs1006899
1000 genomesrs1006899
hgdprs1006899
ensemblrs1006899
gopubmedrs1006899
geneviewrs1006899
scholarrs1006899
googlers1006899
pharmgkbrs1006899
gwascentralrs1006899
openSNPrs1006899
23andMers1006899
23andMe allrs1006899
SNP Nexus

SNPshotrs1006899
SNPdbers1006899
MSV3drs1006899
GWAS Ctlgrs1006899
GMAF0.1405
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19079262]
Trait Bone mineral density (spine)
Title New sequence variants associated with bone mineral density
Risk Allele A
P-val 0.000006
Odds Ratio 0.09 [0.05-0.13] SD decrease

[PMID 19629617OA-icon.png] Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening.


GET Evidence
rs1006899
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.173077
summary