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rs11886047

From SNPedia

Orientationplus
Stabilizedplus
Make rs11886047(C;C)
Make rs11886047(C;T)
Make rs11886047(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position43623451
is asnp
is mentioned by
dbSNPrs11886047
ebirs11886047
HLIrs11886047
Exacrs11886047
Varsomers11886047
Maprs11886047
PheGenIrs11886047
hapmaprs11886047
1000 genomesrs11886047
hgdprs11886047
ensemblrs11886047
gopubmedrs11886047
geneviewrs11886047
scholarrs11886047
googlers11886047
pharmgkbrs11886047
gwascentralrs11886047
openSNPrs11886047
23andMers11886047
23andMe allrs11886047
SNP Nexus

SNPshotrs11886047
SNPdbers11886047
MSV3drs11886047
GWAS Ctlgrs11886047
GMAF0.1387
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 18752002] rs11886047 diabetic nephropathy in 112 cases and 148 controls rs1368086 and rs725238
OMIM603933
DescMICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1; MVCD1
Variant
Relatedalso