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rs9406328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0 common in complete genomics
Make rs9406328(A;A)
Make rs9406328(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position169234915
GeneTHBS2
is asnp
is mentioned by
dbSNPrs9406328
ebirs9406328
HLIrs9406328
Exacrs9406328
Varsomers9406328
Maprs9406328
PheGenIrs9406328
hapmaprs9406328
1000 genomesrs9406328
hgdprs9406328
ensemblrs9406328
gopubmedrs9406328
geneviewrs9406328
scholarrs9406328
googlers9406328
pharmgkbrs9406328
gwascentralrs9406328
openSNPrs9406328
23andMers9406328
23andMe allrs9406328
SNP Nexus

SNPshotrs9406328
SNPdbers9406328
MSV3drs9406328
GWAS Ctlgrs9406328
GMAF0.3503
Max Magnitude0
[PMID 18455130OA-icon.png] (IVS10-8C T; rs9406328) and (Q279R; rs17576) showed significant association with lumbar-disc herniation (odds ratio 3.03, 95% confidence interval 1.58-5.77)
OMIM603932
DescINTERVERTEBRAL DISC DISEASE; IDD
Variant
Relatedalso
OMIM120361
DescMATRIX METALLOPROTEINASE 9; MMP9
Variant
Relatedalso
OMIM188061
DescTHROMBOSPONDIN II; THBS2
Variant
Relatedalso


OMIM188061
Desc
Variant0001
Relatedalso


GET Evidence
rs9406328
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.301692
summary