rs80356635
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs80356635(C;C) |
| Make rs80356635(C;T) |
| Reference | GRCh37 37.1/132 |
| Chromosome | 11 |
| Position | 17496466 |
| Gene | ABCC8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80356635 |
| dbSNP (classic) | rs80356635 |
| ClinGen | rs80356635 |
| ebi | rs80356635 |
| HLI | rs80356635 |
| Exac | rs80356635 |
| Gnomad | rs80356635 |
| Varsome | rs80356635 |
| LitVar | rs80356635 |
| Map | rs80356635 |
| PheGenI | rs80356635 |
| Biobank | rs80356635 |
| 1000 genomes | rs80356635 |
| hgdp | rs80356635 |
| ensembl | rs80356635 |
| geneview | rs80356635 |
| scholar | rs80356635 |
| rs80356635 | |
| pharmgkb | rs80356635 |
| gwascentral | rs80356635 |
| openSNP | rs80356635 |
| 23andMe | rs80356635 |
| SNPshot | rs80356635 |
| SNPdbe | rs80356635 |
| MSV3d | rs80356635 |
| GWAS Ctlg | rs80356635 |
| Status | Deleted |
| Max Magnitude | 0 |
[PMID 17668386
] Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
