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rs9488238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs9488238(A;G)
Make rs9488238(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position113695931
GeneVN1R13P
is asnp
is mentioned by
dbSNPrs9488238
ebirs9488238
HLIrs9488238
Exacrs9488238
Varsomers9488238
Maprs9488238
PheGenIrs9488238
hapmaprs9488238
1000 genomesrs9488238
hgdprs9488238
ensemblrs9488238
gopubmedrs9488238
geneviewrs9488238
scholarrs9488238
googlers9488238
pharmgkbrs9488238
gwascentralrs9488238
openSNPrs9488238
23andMers9488238
23andMe allrs9488238
SNP Nexus

SNPshotrs9488238
SNPdbers9488238
MSV3drs9488238
GWAS Ctlgrs9488238
GMAF0.03765
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22993228OA-icon.png]
Trait Disc degeneration (lumbar)
Title Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.
Risk Allele A
P-val 5E-6
Odds Ratio .28 [0.16-0.40] unit decrease