rs879254316
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs879254316(A;A) |
| Make rs879254316(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 5 |
| Position | 149041411 |
| Gene | SH3TC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs879254316 |
| dbSNP (classic) | rs879254316 |
| ClinGen | rs879254316 |
| ebi | rs879254316 |
| HLI | rs879254316 |
| Exac | rs879254316 |
| Gnomad | rs879254316 |
| Varsome | rs879254316 |
| LitVar | rs879254316 |
| Map | rs879254316 |
| PheGenI | rs879254316 |
| Biobank | rs879254316 |
| 1000 genomes | rs879254316 |
| hgdp | rs879254316 |
| ensembl | rs879254316 |
| geneview | rs879254316 |
| scholar | rs879254316 |
| rs879254316 | |
| pharmgkb | rs879254316 |
| gwascentral | rs879254316 |
| openSNP | rs879254316 |
| 23andMe | rs879254316 |
| SNPshot | rs879254316 |
| SNPdbe | rs879254316 |
| MSV3d | rs879254316 |
| GWAS Ctlg | rs879254316 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs879254316(A;A) |
| Alt | rs879254316(A;A) |
| Reference | Rs879254316(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SH3TC2 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000005.9:g.148420974C>T |
| CLNSRC | |
| CLNACC | RCV000236994.1, |
