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rs10998466

From SNPedia

Orientationplus
Stabilizedplus
Make rs10998466(A;A)
Make rs10998466(A;G)
Make rs10998466(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position68866673
GeneSTOX1
is asnp
is mentioned by
dbSNPrs10998466
ebirs10998466
HLIrs10998466
Exacrs10998466
Varsomers10998466
Maprs10998466
PheGenIrs10998466
hapmaprs10998466
1000 genomesrs10998466
hgdprs10998466
ensemblrs10998466
gopubmedrs10998466
geneviewrs10998466
scholarrs10998466
googlers10998466
pharmgkbrs10998466
gwascentralrs10998466
openSNPrs10998466
23andMers10998466
23andMe allrs10998466
SNP Nexus

SNPshotrs10998466
SNPdbers10998466
MSV3drs10998466
GWAS Ctlgrs10998466
GMAF0.03581
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 4E-6
Odds Ratio .53 [0.31-0.75] unit decrease