rs34154371
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs34154371(A;G) |
| Make rs34154371(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 2406576 |
| Gene | PEX10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34154371 |
| dbSNP (classic) | rs34154371 |
| ClinGen | rs34154371 |
| ebi | rs34154371 |
| HLI | rs34154371 |
| Exac | rs34154371 |
| Gnomad | rs34154371 |
| Varsome | rs34154371 |
| LitVar | rs34154371 |
| Map | rs34154371 |
| PheGenI | rs34154371 |
| Biobank | rs34154371 |
| 1000 genomes | rs34154371 |
| hgdp | rs34154371 |
| ensembl | rs34154371 |
| geneview | rs34154371 |
| scholar | rs34154371 |
| rs34154371 | |
| pharmgkb | rs34154371 |
| gwascentral | rs34154371 |
| openSNP | rs34154371 |
| 23andMe | rs34154371 |
| SNPshot | rs34154371 |
| SNPdbe | rs34154371 |
| MSV3d | rs34154371 |
| GWAS Ctlg | rs34154371 |
| GMAF | 0.009642 |
| Max Magnitude | 0 |
[PMID 15542397] The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.
| ClinVar | |
|---|---|
| Risk | rs34154371(G;G) |
| Alt | rs34154371(G;G) |
| Reference | Rs34154371(A;A) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | PEX10 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000001.10:g.2338015T>C |
| CLNSRC | |
| CLNACC | RCV000179027.2, |
