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rs5029928

From SNPedia

Orientationplus
Stabilizedplus
Make rs5029928(C;C)
Make rs5029928(C;T)
Make rs5029928(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137868805
GeneLOC100130476, TNFAIP3
is asnp
is mentioned by
dbSNPrs5029928
dbSNP (classic)rs5029928
ClinGenrs5029928
ebirs5029928
HLIrs5029928
Exacrs5029928
Gnomadrs5029928
Varsomers5029928
LitVarrs5029928
Maprs5029928
PheGenIrs5029928
Biobankrs5029928
1000 genomesrs5029928
hgdprs5029928
ensemblrs5029928
geneviewrs5029928
scholarrs5029928
googlers5029928
pharmgkbrs5029928
gwascentralrs5029928
openSNPrs5029928
23andMers5029928
SNPshotrs5029928
SNPdbers5029928
MSV3drs5029928
GWAS Ctlgrs5029928
GMAF0.1837
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23161053] TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population