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rs1029295

From SNPedia

Orientationminus
Stabilizedminus
Make rs1029295(A;A)
Make rs1029295(A;G)
Make rs1029295(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32888705
is asnp
is mentioned by
dbSNPrs1029295
dbSNP (classic)rs1029295
ClinGenrs1029295
ebirs1029295
HLIrs1029295
Exacrs1029295
Gnomadrs1029295
Varsomers1029295
LitVarrs1029295
Maprs1029295
PheGenIrs1029295
Biobankrs1029295
1000 genomesrs1029295
hgdprs1029295
ensemblrs1029295
geneviewrs1029295
scholarrs1029295
googlers1029295
pharmgkbrs1029295
gwascentralrs1029295
openSNPrs1029295
23andMers1029295
SNPshotrs1029295
SNPdbers1029295
MSV3drs1029295
GWAS Ctlgrs1029295
GMAF0.1235
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 C
P-val 5E-7
Odds Ratio .19 [0.12-0.26] unit increase