rs28933690
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (T;T) | 0 | common in clinvar |
| Make rs28933690(C;C) |
| Make rs28933690(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | X |
| Position | 37728007 |
| Gene | XK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28933690 |
| dbSNP (classic) | rs28933690 |
| ClinGen | rs28933690 |
| ebi | rs28933690 |
| HLI | rs28933690 |
| Exac | rs28933690 |
| Gnomad | rs28933690 |
| Varsome | rs28933690 |
| LitVar | rs28933690 |
| Map | rs28933690 |
| PheGenI | rs28933690 |
| Biobank | rs28933690 |
| 1000 genomes | rs28933690 |
| hgdp | rs28933690 |
| ensembl | rs28933690 |
| geneview | rs28933690 |
| scholar | rs28933690 |
| rs28933690 | |
| pharmgkb | rs28933690 |
| gwascentral | rs28933690 |
| openSNP | rs28933690 |
| 23andMe | rs28933690 |
| SNPshot | rs28933690 |
| SNPdbe | rs28933690 |
| MSV3d | rs28933690 |
| GWAS Ctlg | rs28933690 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28933690(G;G) |
| Alt | rs28933690(G;G) |
| Reference | Rs28933690(A;A) |
| Significance | Pathogenic |
| Disease | McLeod neuroacanthocytosis syndrome |
| Variation | info |
| Gene | XK |
| CLNDBN | McLeod neuroacanthocytosis syndrome |
| Reversed | 1 |
| HGVS | NC_000023.10:g.37587260T>C |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000010422.3, |
