rs770674400
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs770674400(G;T) |
| Make rs770674400(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 75022145 |
| Gene | KAT6B, SNORD172 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs770674400 |
| dbSNP (classic) | rs770674400 |
| ClinGen | rs770674400 |
| ebi | rs770674400 |
| HLI | rs770674400 |
| Exac | rs770674400 |
| Gnomad | rs770674400 |
| Varsome | rs770674400 |
| LitVar | rs770674400 |
| Map | rs770674400 |
| PheGenI | rs770674400 |
| Biobank | rs770674400 |
| 1000 genomes | rs770674400 |
| hgdp | rs770674400 |
| ensembl | rs770674400 |
| geneview | rs770674400 |
| scholar | rs770674400 |
| rs770674400 | |
| pharmgkb | rs770674400 |
| gwascentral | rs770674400 |
| openSNP | rs770674400 |
| 23andMe | rs770674400 |
| SNPshot | rs770674400 |
| SNPdbe | rs770674400 |
| MSV3d | rs770674400 |
| GWAS Ctlg | rs770674400 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs770674400(A;A) rs770674400(T;T) |
| Alt | rs770674400(A;A) rs770674400(T;T) |
| Reference | Rs770674400(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | KAT6B |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.76781903G>T |
| CLNSRC | |
| CLNACC | RCV000484958.1, |
