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