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rs2017567

From SNPedia

Orientationplus
Stabilizedplus
Make rs2017567(C;C)
Make rs2017567(C;T)
Make rs2017567(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position587212
is asnp
is mentioned by
dbSNPrs2017567
ebirs2017567
HLIrs2017567
Exacrs2017567
Varsomers2017567
Maprs2017567
PheGenIrs2017567
hapmaprs2017567
1000 genomesrs2017567
hgdprs2017567
ensemblrs2017567
gopubmedrs2017567
geneviewrs2017567
scholarrs2017567
googlers2017567
pharmgkbrs2017567
gwascentralrs2017567
openSNPrs2017567
23andMers2017567
23andMe allrs2017567
SNP Nexus

SNPshotrs2017567
SNPdbers2017567
MSV3drs2017567
GWAS Ctlgrs2017567
GMAF0.478
Max Magnitude
? (C;C) (C;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 C
P-val 9E-6
Odds Ratio .10 [0.059-0.141] unit increase