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rs878962

From SNPedia

Orientationminus
Stabilizedminus
Make rs878962(A;A)
Make rs878962(A;C)
Make rs878962(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position3178113
GeneTSPAN9
is asnp
is mentioned by
dbSNPrs878962
ebirs878962
HLIrs878962
Exacrs878962
Varsomers878962
Maprs878962
PheGenIrs878962
hapmaprs878962
1000 genomesrs878962
hgdprs878962
ensemblrs878962
gopubmedrs878962
geneviewrs878962
scholarrs878962
googlers878962
pharmgkbrs878962
gwascentralrs878962
openSNPrs878962
23andMers878962
23andMe allrs878962
SNP Nexus

SNPshotrs878962
SNPdbers878962
MSV3drs878962
GWAS Ctlgrs878962
GMAF0.4913
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23746317]
Trait Temporomandibular joint disorders
Title Genome-wide association study of degenerative bony changes of the temporomandibular joint.
Risk Allele C
P-val 8E-6
Odds Ratio 1.89 [1.43-2.50]