rs1411766
| Orientation | minus |
| Stabilized | minus |
| Make rs1411766(C;C) |
| Make rs1411766(C;T) |
| Make rs1411766(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 109599813 |
| Gene | LOC101927627 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1411766 |
| dbSNP (classic) | rs1411766 |
| ClinGen | rs1411766 |
| ebi | rs1411766 |
| HLI | rs1411766 |
| Exac | rs1411766 |
| Gnomad | rs1411766 |
| Varsome | rs1411766 |
| LitVar | rs1411766 |
| Map | rs1411766 |
| PheGenI | rs1411766 |
| Biobank | rs1411766 |
| 1000 genomes | rs1411766 |
| hgdp | rs1411766 |
| ensembl | rs1411766 |
| geneview | rs1411766 |
| scholar | rs1411766 |
| rs1411766 | |
| pharmgkb | rs1411766 |
| gwascentral | rs1411766 |
| openSNP | rs1411766 |
| 23andMe | rs1411766 |
| SNPshot | rs1411766 |
| SNPdbe | rs1411766 |
| MSV3d | rs1411766 |
| GWAS Ctlg | rs1411766 |
| GMAF | 0.2089 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20460425
] 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 19252134
] Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.
[PMID 19924099
] Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scan.
[PMID 20835900
] Genetics of diabetes complications.
[PMID 21412220
] An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes.
[PMID 25646961
] 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
- Is a snp
- In dbSNP
- SNPs on chromosome 13
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d
