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rs1054611

From SNPedia

Orientationplus
Stabilizedplus
Make rs1054611(G;G)
Make rs1054611(G;T)
Make rs1054611(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position10017562
GeneCLEC12B
is asnp
is mentioned by
dbSNPrs1054611
ebirs1054611
HLIrs1054611
Exacrs1054611
Varsomers1054611
Maprs1054611
PheGenIrs1054611
hapmaprs1054611
1000 genomesrs1054611
hgdprs1054611
ensemblrs1054611
gopubmedrs1054611
geneviewrs1054611
scholarrs1054611
googlers1054611
pharmgkbrs1054611
gwascentralrs1054611
openSNPrs1054611
23andMers1054611
23andMe allrs1054611
SNP Nexus

SNPshotrs1054611
SNPdbers1054611
MSV3drs1054611
GWAS Ctlgrs1054611
GMAF0.4555
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23834954OA-icon.png]
Trait Sensory disturbances after bilateral sagittal split ramus osteotomy
Title Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.
Risk Allele
P-val 6E-6
Odds Ratio NR NR