rs868197660
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs868197660(A;A) |
| Make rs868197660(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 9 |
| Position | 4117797 |
| Gene | GLIS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs868197660 |
| dbSNP (classic) | rs868197660 |
| ClinGen | rs868197660 |
| ebi | rs868197660 |
| HLI | rs868197660 |
| Exac | rs868197660 |
| Gnomad | rs868197660 |
| Varsome | rs868197660 |
| LitVar | rs868197660 |
| Map | rs868197660 |
| PheGenI | rs868197660 |
| Biobank | rs868197660 |
| 1000 genomes | rs868197660 |
| hgdp | rs868197660 |
| ensembl | rs868197660 |
| geneview | rs868197660 |
| scholar | rs868197660 |
| rs868197660 | |
| pharmgkb | rs868197660 |
| gwascentral | rs868197660 |
| openSNP | rs868197660 |
| 23andMe | rs868197660 |
| SNPshot | rs868197660 |
| SNPdbe | rs868197660 |
| MSV3d | rs868197660 |
| GWAS Ctlg | rs868197660 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs868197660(A;A) |
| Alt | rs868197660(A;A) |
| Reference | Rs868197660(G;G) |
| Significance | Pathogenic |
| Disease | Diabetes mellitus |
| Variation | info |
| Gene | GLIS3 |
| CLNDBN | Diabetes mellitus, neonatal, with congenital hypothyroidism |
| Reversed | 0 |
| HGVS | NC_000009.11:g.4117797G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000239596.1, |
