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rs6457690

From SNPedia

Orientationplus
Stabilizedplus
Make rs6457690(A;A)
Make rs6457690(A;G)
Make rs6457690(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32887940
is asnp
is mentioned by
dbSNPrs6457690
dbSNP (classic)rs6457690
ClinGenrs6457690
ebirs6457690
HLIrs6457690
Exacrs6457690
Gnomadrs6457690
Varsomers6457690
LitVarrs6457690
Maprs6457690
PheGenIrs6457690
Biobankrs6457690
1000 genomesrs6457690
hgdprs6457690
ensemblrs6457690
geneviewrs6457690
scholarrs6457690
googlers6457690
pharmgkbrs6457690
gwascentralrs6457690
openSNPrs6457690
23andMers6457690
SNPshotrs6457690
SNPdbers6457690
MSV3drs6457690
GWAS Ctlgrs6457690
GMAF0.1253
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-8
Odds Ratio .19 [0.12-0.26] unit increase