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rs12722877

From SNPedia

Merged intors2228567
Orientationminus
Stabilizedplus
Make rs12722877(C;C)
Make rs12722877(C;G)
Make rs12722877(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position40307451
GeneCOL9A2
is asnp
is mentioned by
dbSNPrs12722877
ebirs12722877
HLIrs12722877
Exacrs12722877
Varsomers12722877
Maprs12722877
PheGenIrs12722877
hapmaprs12722877
1000 genomesrs12722877
hgdprs12722877
ensemblrs12722877
gopubmedrs12722877
geneviewrs12722877
scholarrs12722877
googlers12722877
pharmgkbrs12722877
gwascentralrs12722877
openSNPrs12722877
23andMers12722877
23andMe allrs12722877
SNP Nexus

SNPshotrs12722877
SNPdbers12722877
MSV3drs12722877
GWAS Ctlgrs12722877
StatusMerged into rs2228567
Max Magnitude
Venter snp
Source plos
Gene COL9A2
allele C
frequency
sift TOLERATED
HuRef 1103675074802
Disease Association Defects in COL9A2 may be a cause of susceptibility to intervertebral disc disease (IDD) (MIM:603932). IDD is one of the most common musculo-skeletal disorders.



[PMID 24983932] Meta-Analysis of the Association Between COL9A2 Genetic Polymorphisms and Lumbar Disc Disease Susceptibility