rs35082957
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs35082957(A;A) |
| Make rs35082957(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 2406553 |
| Gene | PEX10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35082957 |
| dbSNP (classic) | rs35082957 |
| ClinGen | rs35082957 |
| ebi | rs35082957 |
| HLI | rs35082957 |
| Exac | rs35082957 |
| Gnomad | rs35082957 |
| Varsome | rs35082957 |
| LitVar | rs35082957 |
| Map | rs35082957 |
| PheGenI | rs35082957 |
| Biobank | rs35082957 |
| 1000 genomes | rs35082957 |
| hgdp | rs35082957 |
| ensembl | rs35082957 |
| geneview | rs35082957 |
| scholar | rs35082957 |
| rs35082957 | |
| pharmgkb | rs35082957 |
| gwascentral | rs35082957 |
| openSNP | rs35082957 |
| 23andMe | rs35082957 |
| SNPshot | rs35082957 |
| SNPdbe | rs35082957 |
| MSV3d | rs35082957 |
| GWAS Ctlg | rs35082957 |
| GMAF | 0.003214 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35082957(A;A) |
| Alt | rs35082957(A;A) |
| Reference | Rs35082957(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified Zellweger syndrome |
| Variation | info |
| Gene | PEX10 |
| CLNDBN | not specified Zellweger syndrome |
| Reversed | 1 |
| HGVS | NC_000001.10:g.2337992C>T |
| CLNSRC | Illumina |
| CLNACC | RCV000247875.1, RCV000282889.1, |
