rs35897051
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs35897051(A;C) |
| Make rs35897051(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 58270865 |
| Gene | MPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35897051 |
| dbSNP (classic) | rs35897051 |
| ClinGen | rs35897051 |
| ebi | rs35897051 |
| HLI | rs35897051 |
| Exac | rs35897051 |
| Gnomad | rs35897051 |
| Varsome | rs35897051 |
| LitVar | rs35897051 |
| Map | rs35897051 |
| PheGenI | rs35897051 |
| Biobank | rs35897051 |
| 1000 genomes | rs35897051 |
| hgdp | rs35897051 |
| ensembl | rs35897051 |
| geneview | rs35897051 |
| scholar | rs35897051 |
| rs35897051 | |
| pharmgkb | rs35897051 |
| gwascentral | rs35897051 |
| openSNP | rs35897051 |
| 23andMe | rs35897051 |
| SNPshot | rs35897051 |
| SNPdbe | rs35897051 |
| MSV3d | rs35897051 |
| GWAS Ctlg | rs35897051 |
| GMAF | 0.001377 |
| Max Magnitude | 0 |
[PMID 23620142
] Genome-wide and Gene-Centric Analyses of Circulating Myeloperoxidase Levels in the CHARGE and CARe Consortia
| ClinVar | |
|---|---|
| Risk | rs35897051(C;C) |
| Alt | rs35897051(C;C) |
| Reference | Rs35897051(A;A) |
| Significance | Pathogenic |
| Disease | Myeloperoxidase deficiency not provided |
| Variation | info |
| Gene | MPO |
| CLNDBN | Myeloperoxidase deficiency not provided |
| Reversed | 1 |
| HGVS | NC_000017.10:g.56348226T>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000003816.5, RCV000265536.1, |
