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rs6537883

From SNPedia

Orientationplus
Stabilizedplus
Make rs6537883(C;C)
Make rs6537883(C;T)
Make rs6537883(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position109862649
is asnp
is mentioned by
dbSNPrs6537883
ebirs6537883
HLIrs6537883
Exacrs6537883
Varsomers6537883
Maprs6537883
PheGenIrs6537883
hapmaprs6537883
1000 genomesrs6537883
hgdprs6537883
ensemblrs6537883
gopubmedrs6537883
geneviewrs6537883
scholarrs6537883
googlers6537883
pharmgkbrs6537883
gwascentralrs6537883
openSNPrs6537883
23andMers6537883
23andMe allrs6537883
SNP Nexus

SNPshotrs6537883
SNPdbers6537883
MSV3drs6537883
GWAS Ctlgrs6537883
GMAF0.4656
Max Magnitude
? (C;C) (C;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 3E-6
Odds Ratio NR NR