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rs17034687

From SNPedia

Orientationplus
Stabilizedplus
Make rs17034687(C;C)
Make rs17034687(C;G)
Make rs17034687(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position3638168
is asnp
is mentioned by
dbSNPrs17034687
ebirs17034687
HLIrs17034687
Exacrs17034687
Varsomers17034687
Maprs17034687
PheGenIrs17034687
hapmaprs17034687
1000 genomesrs17034687
hgdprs17034687
ensemblrs17034687
gopubmedrs17034687
geneviewrs17034687
scholarrs17034687
googlers17034687
pharmgkbrs17034687
gwascentralrs17034687
openSNPrs17034687
23andMers17034687
23andMe allrs17034687
SNP Nexus

SNPshotrs17034687
SNPdbers17034687
MSV3drs17034687
GWAS Ctlgrs17034687
GMAF0.05877
Max Magnitude
? (C;C) (C;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 C
P-val 2E-9
Odds Ratio .23 [0.16-0.30] unit increase