rs1801262
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1801262(A;A) |
| Make rs1801262(A;G) |
| Make rs1801262(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 181678728 |
| Gene | NEUROD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1801262 |
| dbSNP (classic) | rs1801262 |
| ClinGen | rs1801262 |
| ebi | rs1801262 |
| HLI | rs1801262 |
| Exac | rs1801262 |
| Gnomad | rs1801262 |
| Varsome | rs1801262 |
| LitVar | rs1801262 |
| Map | rs1801262 |
| PheGenI | rs1801262 |
| Biobank | rs1801262 |
| 1000 genomes | rs1801262 |
| hgdp | rs1801262 |
| ensembl | rs1801262 |
| geneview | rs1801262 |
| scholar | rs1801262 |
| rs1801262 | |
| pharmgkb | rs1801262 |
| gwascentral | rs1801262 |
| openSNP | rs1801262 |
| 23andMe | rs1801262 |
| SNPshot | rs1801262 |
| SNPdbe | rs1801262 |
| MSV3d | rs1801262 |
| GWAS Ctlg | rs1801262 |
| GMAF | 0.2658 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| Rs1801262 | |
|---|---|
| PubMed | [PMID 17192490] |
| Affy Probeset | SNP_A-2314121 |
| Affy Orientation | same |
| On GW 5.0 | 1 |
| Alleles A/B | A/G |
| Ancestral | G |
| Population | NEU(Finnland) |
| Allele | A |
| Case Freq. | 0.37 |
| Control Freq. | 0.34 |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.15 |
| Disease | Type II Diabetes (T2D) |
rs1801262 increases susceptibility to Type II Diabetes 1.15 times for carriers of the A allele [PMID 17192490]
[PMID 14681825
] Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
[PMID 16909454
] NeuroD1 gene and interleukin-18 gene polymorphisms in type 1 diabetes in Dalmatian population of Southern Croatia.
[PMID 20416077
] Identification of type 2 diabetes-associated combination of SNPs using support vector machine.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- Has Report GE
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
