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rs11969002

From SNPedia

Orientationplus
Stabilizedplus
Make rs11969002(A;A)
Make rs11969002(A;G)
Make rs11969002(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32891971
is asnp
is mentioned by
dbSNPrs11969002
ebirs11969002
HLIrs11969002
Exacrs11969002
Varsomers11969002
Maprs11969002
PheGenIrs11969002
hapmaprs11969002
1000 genomesrs11969002
hgdprs11969002
ensemblrs11969002
gopubmedrs11969002
geneviewrs11969002
scholarrs11969002
googlers11969002
pharmgkbrs11969002
gwascentralrs11969002
openSNPrs11969002
23andMers11969002
23andMe allrs11969002
SNP Nexus

SNPshotrs11969002
SNPdbers11969002
MSV3drs11969002
GWAS Ctlgrs11969002
GMAF0.112
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 6E-8
Odds Ratio .20 [0.13-0.27] unit increase