rs387906631
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs387906631(C;T) |
| Make rs387906631(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 128481901 |
| Gene | GATA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs387906631 |
| dbSNP (classic) | rs387906631 |
| ClinGen | rs387906631 |
| ebi | rs387906631 |
| HLI | rs387906631 |
| Exac | rs387906631 |
| Gnomad | rs387906631 |
| Varsome | rs387906631 |
| LitVar | rs387906631 |
| Map | rs387906631 |
| PheGenI | rs387906631 |
| Biobank | rs387906631 |
| 1000 genomes | rs387906631 |
| hgdp | rs387906631 |
| ensembl | rs387906631 |
| geneview | rs387906631 |
| scholar | rs387906631 |
| rs387906631 | |
| pharmgkb | rs387906631 |
| gwascentral | rs387906631 |
| openSNP | rs387906631 |
| 23andMe | rs387906631 |
| SNPshot | rs387906631 |
| SNPdbe | rs387906631 |
| MSV3d | rs387906631 |
| GWAS Ctlg | rs387906631 |
| Max Magnitude | 0 |
aka NM_001145661.1(GATA2):c.1061C>T or (p.Thr354Met)
OMIM pathogenic variant
