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rs2484992

From SNPedia

Orientationminus
Stabilizedminus
Make rs2484992(A;A)
Make rs2484992(A;G)
Make rs2484992(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position31223169
GeneLOC101929352
is asnp
is mentioned by
dbSNPrs2484992
ebirs2484992
HLIrs2484992
Exacrs2484992
Varsomers2484992
Maprs2484992
PheGenIrs2484992
hapmaprs2484992
1000 genomesrs2484992
hgdprs2484992
ensemblrs2484992
gopubmedrs2484992
geneviewrs2484992
scholarrs2484992
googlers2484992
pharmgkbrs2484992
gwascentralrs2484992
openSNPrs2484992
23andMers2484992
23andMe allrs2484992
SNP Nexus

SNPshotrs2484992
SNPdbers2484992
MSV3drs2484992
GWAS Ctlgrs2484992
GMAF0.2374
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 5E-6
Odds Ratio .68 [0.39-0.97] unit increase