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rs1029296

From SNPedia

Orientationminus
Stabilizedminus
Make rs1029296(A;A)
Make rs1029296(A;G)
Make rs1029296(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32888604
is asnp
is mentioned by
dbSNPrs1029296
ebirs1029296
HLIrs1029296
Exacrs1029296
Varsomers1029296
Maprs1029296
PheGenIrs1029296
hapmaprs1029296
1000 genomesrs1029296
hgdprs1029296
ensemblrs1029296
gopubmedrs1029296
geneviewrs1029296
scholarrs1029296
googlers1029296
pharmgkbrs1029296
gwascentralrs1029296
openSNPrs1029296
23andMers1029296
23andMe allrs1029296
SNP Nexus

SNPshotrs1029296
SNPdbers1029296
MSV3drs1029296
GWAS Ctlgrs1029296
GMAF0.1235
Max Magnitude
? (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 C
P-val 9E-8
Odds Ratio .19 [0.12-0.26] unit increase