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rs17053082

From SNPedia

Orientationplus
Stabilizedplus
Make rs17053082(C;C)
Make rs17053082(C;T)
Make rs17053082(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position155967220
is asnp
is mentioned by
dbSNPrs17053082
ebirs17053082
HLIrs17053082
Exacrs17053082
Varsomers17053082
Maprs17053082
PheGenIrs17053082
hapmaprs17053082
1000 genomesrs17053082
hgdprs17053082
ensemblrs17053082
gopubmedrs17053082
geneviewrs17053082
scholarrs17053082
googlers17053082
pharmgkbrs17053082
gwascentralrs17053082
openSNPrs17053082
23andMers17053082
23andMe allrs17053082
SNP Nexus

SNPshotrs17053082
SNPdbers17053082
MSV3drs17053082
GWAS Ctlgrs17053082
GMAF0.06015
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23300278OA-icon.png]
Trait Type 2 diabetes
Title Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India.
Risk Allele T
P-val 4E-7
Odds Ratio 1.49 [1.28 - 1.73]