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rs12805875

From SNPedia

Orientationplus
Stabilizedplus
Make rs12805875(A;A)
Make rs12805875(A;G)
Make rs12805875(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position103658904
is asnp
is mentioned by
dbSNPrs12805875
dbSNP (classic)rs12805875
ClinGenrs12805875
ebirs12805875
HLIrs12805875
Exacrs12805875
Gnomadrs12805875
Varsomers12805875
LitVarrs12805875
Maprs12805875
PheGenIrs12805875
Biobankrs12805875
1000 genomesrs12805875
hgdprs12805875
ensemblrs12805875
geneviewrs12805875
scholarrs12805875
googlers12805875
pharmgkbrs12805875
gwascentralrs12805875
openSNPrs12805875
23andMers12805875
SNPshotrs12805875
SNPdbers12805875
MSV3drs12805875
GWAS Ctlgrs12805875
GMAF0.4725
Max Magnitude0
? (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 increse