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rs10214886

From SNPedia

Orientationplus
Stabilizedplus
Make rs10214886(A;A)
Make rs10214886(A;T)
Make rs10214886(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32889642
is asnp
is mentioned by
dbSNPrs10214886
ebirs10214886
HLIrs10214886
Exacrs10214886
Varsomers10214886
Maprs10214886
PheGenIrs10214886
hapmaprs10214886
1000 genomesrs10214886
hgdprs10214886
ensemblrs10214886
gopubmedrs10214886
geneviewrs10214886
scholarrs10214886
googlers10214886
pharmgkbrs10214886
gwascentralrs10214886
openSNPrs10214886
23andMers10214886
23andMe allrs10214886
SNP Nexus

SNPshotrs10214886
SNPdbers10214886
MSV3drs10214886
GWAS Ctlgrs10214886
GMAF0.1272
Max Magnitude
? (A;A) (A;T) (T;T) 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 2E-7
Odds Ratio .19 [0.12-0.26] unit increase