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rs1411766

From SNPedia

Orientationminus
Stabilizedminus
Make rs1411766(C;C)
Make rs1411766(C;T)
Make rs1411766(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position109599813
GeneLOC101927627
is asnp
is mentioned by
dbSNPrs1411766
dbSNP (classic)rs1411766
ClinGenrs1411766
ebirs1411766
HLIrs1411766
Exacrs1411766
Gnomadrs1411766
Varsomers1411766
LitVarrs1411766
Maprs1411766
PheGenIrs1411766
Biobankrs1411766
1000 genomesrs1411766
hgdprs1411766
ensemblrs1411766
geneviewrs1411766
scholarrs1411766
googlers1411766
pharmgkbrs1411766
gwascentralrs1411766
openSNPrs1411766
23andMers1411766
SNPshotrs1411766
SNPdbers1411766
MSV3drs1411766
GWAS Ctlgrs1411766
GMAF0.2089
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20460425OA-icon.png] the rs1411766 locus may be commonly involved in conferring susceptibility to diabetic nephropathy among subjects with type 1 or type 2 diabetes across different ethnic groups.


[PMID 19252134OA-icon.png] Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.


[PMID 19924099OA-icon.png] Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scan.


[PMID 20835900OA-icon.png] Genetics of diabetes complications.


[PMID 21412220OA-icon.png] An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes.


[PMID 25646961OA-icon.png] Identification of an Interaction between VWF rs7965413 and Platelet Count as a Novel Risk Marker for Metabolic Syndrome: An Extensive Search of Candidate Polymorphisms in a Case-Control Study