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rs7744666

From SNPedia

Orientationplus
Stabilizedplus
Make rs7744666(C;C)
Make rs7744666(C;T)
Make rs7744666(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32891935
is asnp
is mentioned by
dbSNPrs7744666
ebirs7744666
HLIrs7744666
Exacrs7744666
Varsomers7744666
Maprs7744666
PheGenIrs7744666
hapmaprs7744666
1000 genomesrs7744666
hgdprs7744666
ensemblrs7744666
gopubmedrs7744666
geneviewrs7744666
scholarrs7744666
googlers7744666
pharmgkbrs7744666
gwascentralrs7744666
openSNPrs7744666
23andMers7744666
23andMe allrs7744666
SNP Nexus

SNPshotrs7744666
SNPdbers7744666
MSV3drs7744666
GWAS Ctlgrs7744666
GMAF0.1125
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 6E-8
Odds Ratio .20 [0.13-0.27] unit increase