rs876660979
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs876660979(A;A) |
| Make rs876660979(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 10658467 |
| Gene | JAG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876660979 |
| dbSNP (classic) | rs876660979 |
| ClinGen | rs876660979 |
| ebi | rs876660979 |
| HLI | rs876660979 |
| Exac | rs876660979 |
| Gnomad | rs876660979 |
| Varsome | rs876660979 |
| LitVar | rs876660979 |
| Map | rs876660979 |
| PheGenI | rs876660979 |
| Biobank | rs876660979 |
| 1000 genomes | rs876660979 |
| hgdp | rs876660979 |
| ensembl | rs876660979 |
| geneview | rs876660979 |
| scholar | rs876660979 |
| rs876660979 | |
| pharmgkb | rs876660979 |
| gwascentral | rs876660979 |
| openSNP | rs876660979 |
| 23andMe | rs876660979 |
| SNPshot | rs876660979 |
| SNPdbe | rs876660979 |
| MSV3d | rs876660979 |
| GWAS Ctlg | rs876660979 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876660979(A;A) |
| Alt | rs876660979(A;A) |
| Reference | Rs876660979(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | JAG1 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000020.10:g.10639115C>T |
| CLNSRC | |
| CLNACC | RCV000216385.1, |
