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rs2063640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2063640(A;A)
Make rs2063640(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position102484201
is asnp
is mentioned by
dbSNPrs2063640
dbSNP (classic)rs2063640
ClinGenrs2063640
ebirs2063640
HLIrs2063640
Exacrs2063640
Gnomadrs2063640
Varsomers2063640
LitVarrs2063640
Maprs2063640
PheGenIrs2063640
Biobankrs2063640
1000 genomesrs2063640
hgdprs2063640
ensemblrs2063640
geneviewrs2063640
scholarrs2063640
googlers2063640
pharmgkbrs2063640
gwascentralrs2063640
openSNPrs2063640
23andMers2063640
SNPshotrs2063640
SNPdbers2063640
MSV3drs2063640
GWAS Ctlgrs2063640
GMAF0.1621
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 21490949OA-icon.png]
Trait
Title Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
Risk Allele A
P-val 0.000003
Odds Ratio 1.2300 [1.13-1.34]


[PMID 23834954OA-icon.png] Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy