rs1801239
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common on affy axiom data |
(T;T) | 0 |
Make rs1801239(A;G) |
Make rs1801239(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 16877053 |
Gene | CUBN |
is a | snp |
is | mentioned by |
dbSNP | rs1801239 |
dbSNP (classic) | rs1801239 |
ClinGen | rs1801239 |
ebi | rs1801239 |
HLI | rs1801239 |
Exac | rs1801239 |
Gnomad | rs1801239 |
Varsome | rs1801239 |
LitVar | rs1801239 |
Map | rs1801239 |
PheGenI | rs1801239 |
Biobank | rs1801239 |
1000 genomes | rs1801239 |
hgdp | rs1801239 |
ensembl | rs1801239 |
geneview | rs1801239 |
scholar | rs1801239 |
rs1801239 | |
pharmgkb | rs1801239 |
gwascentral | rs1801239 |
openSNP | rs1801239 |
23andMe | rs1801239 |
SNPshot | rs1801239 |
SNPdbe | rs1801239 |
MSV3d | rs1801239 |
GWAS Ctlg | rs1801239 |
GMAF | 0.0528 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21355061] |
Trait | |
Title | CUBN Is a Gene Locus for Albuminuria |
Risk Allele | T |
P-val | 1E-11 |
Odds Ratio | 0.0835 [NR] unit decrease (CKDGen) |
[PMID 22574174] CUBN as a Novel Locus for End-Stage Renal Disease: Insights from Renal Transplantation
[PMID 27197912] Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.
ClinVar | |
---|---|
Risk | rs1801239(G;G) |
Alt | rs1801239(G;G) |
Reference | Rs1801239(A;A) |
Significance | Probable-non-pathogenic |
Disease | Megaloblastic anemia |
Variation | info |
Gene | CUBN |
CLNDBN | Megaloblastic anemia |
Reversed | 1 |
HGVS | NC_000010.10:g.16919052T>C |
CLNSRC | |
CLNACC | RCV000389104.1, |
[PMID 30557881] Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients.