rs58640772
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs58640772(-;-) |
| Make rs58640772(-;GCGCTACGTGGAG) |
| Make rs58640772(GCGCTACGTGGAG;GCGCTACGTGGAG) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 8 |
| Position | 24956455 |
| Gene | NEFL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs58640772 |
| dbSNP (classic) | rs58640772 |
| ClinGen | rs58640772 |
| ebi | rs58640772 |
| HLI | rs58640772 |
| Exac | rs58640772 |
| Gnomad | rs58640772 |
| Varsome | rs58640772 |
| LitVar | rs58640772 |
| Map | rs58640772 |
| PheGenI | rs58640772 |
| Biobank | rs58640772 |
| 1000 genomes | rs58640772 |
| hgdp | rs58640772 |
| ensembl | rs58640772 |
| geneview | rs58640772 |
| scholar | rs58640772 |
| rs58640772 | |
| pharmgkb | rs58640772 |
| gwascentral | rs58640772 |
| openSNP | rs58640772 |
| 23andMe | rs58640772 |
| SNPshot | rs58640772 |
| SNPdbe | rs58640772 |
| MSV3d | rs58640772 |
| GWAS Ctlg | rs58640772 |
| Max Magnitude | 0 |
aka NM_006158.4(NEFL):c.48_60dupGCGCTACGTGGAG or (p.Thr21Alafs)
OMIM pathogenic variant
