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rs7118412

From SNPedia

Orientationplus
Stabilizedplus
Make rs7118412(A;A)
Make rs7118412(A;G)
Make rs7118412(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position103655026
is asnp
is mentioned by
dbSNPrs7118412
ebirs7118412
HLIrs7118412
Exacrs7118412
Varsomers7118412
Maprs7118412
PheGenIrs7118412
hapmaprs7118412
1000 genomesrs7118412
hgdprs7118412
ensemblrs7118412
gopubmedrs7118412
geneviewrs7118412
scholarrs7118412
googlers7118412
pharmgkbrs7118412
gwascentralrs7118412
openSNPrs7118412
23andMers7118412
23andMe allrs7118412
SNP Nexus

SNPshotrs7118412
SNPdbers7118412
MSV3drs7118412
GWAS Ctlgrs7118412
GMAF0.4619
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 9E-6
Odds Ratio .09 [0.049-0.131] unit increase