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rs9317284

From SNPedia

Orientationplus
Stabilizedplus
Make rs9317284(G;G)
Make rs9317284(G;T)
Make rs9317284(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position63060217
is asnp
is mentioned by
dbSNPrs9317284
ebirs9317284
HLIrs9317284
Exacrs9317284
Varsomers9317284
Maprs9317284
PheGenIrs9317284
hapmaprs9317284
1000 genomesrs9317284
hgdprs9317284
ensemblrs9317284
gopubmedrs9317284
geneviewrs9317284
scholarrs9317284
googlers9317284
pharmgkbrs9317284
gwascentralrs9317284
openSNPrs9317284
23andMers9317284
23andMe allrs9317284
SNP Nexus

SNPshotrs9317284
SNPdbers9317284
MSV3drs9317284
GWAS Ctlgrs9317284
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS
SNP rs9317284
PubMedID [PMID 17903296OA-icon.png]
Condition Bone mineral density
Gene Intergenic
Risk Allele
pValue 2.00E-007
OR NA
95% CI



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


GET Evidence
rs9317284
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary