rs200702600
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs200702600(C;T) |
| Make rs200702600(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 32435795 |
| Gene | ASXL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200702600 |
| dbSNP (classic) | rs200702600 |
| ClinGen | rs200702600 |
| ebi | rs200702600 |
| HLI | rs200702600 |
| Exac | rs200702600 |
| Gnomad | rs200702600 |
| Varsome | rs200702600 |
| LitVar | rs200702600 |
| Map | rs200702600 |
| PheGenI | rs200702600 |
| Biobank | rs200702600 |
| 1000 genomes | rs200702600 |
| hgdp | rs200702600 |
| ensembl | rs200702600 |
| geneview | rs200702600 |
| scholar | rs200702600 |
| rs200702600 | |
| pharmgkb | rs200702600 |
| gwascentral | rs200702600 |
| openSNP | rs200702600 |
| 23andMe | rs200702600 |
| SNPshot | rs200702600 |
| SNPdbe | rs200702600 |
| MSV3d | rs200702600 |
| GWAS Ctlg | rs200702600 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs200702600(A;A) rs200702600(T;T) |
| Alt | rs200702600(A;A) rs200702600(T;T) |
| Reference | Rs200702600(C;C) |
| Significance | Pathogenic |
| Disease | C-like syndrome not specified |
| Variation | info |
| Gene | ASXL1 |
| CLNDBN | C-like syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000020.10:g.31023598C>A; NC_000020.10:g.31023598C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000023978.2, RCV000120095.1, |
