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rs10046257

From SNPedia

Orientationplus
Stabilizedplus
Make rs10046257(A;A)
Make rs10046257(A;G)
Make rs10046257(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32886920
is asnp
is mentioned by
dbSNPrs10046257
ebirs10046257
HLIrs10046257
Exacrs10046257
Varsomers10046257
Maprs10046257
PheGenIrs10046257
hapmaprs10046257
1000 genomesrs10046257
hgdprs10046257
ensemblrs10046257
gopubmedrs10046257
geneviewrs10046257
scholarrs10046257
googlers10046257
pharmgkbrs10046257
gwascentralrs10046257
openSNPrs10046257
23andMers10046257
23andMe allrs10046257
SNP Nexus

SNPshotrs10046257
SNPdbers10046257
MSV3drs10046257
GWAS Ctlgrs10046257
GMAF0.1575
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 A
P-val 3E-7
Odds Ratio .19 [0.12-0.26] unit increase