rs386833498
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs386833498(-;-) |
| Make rs386833498(-;A) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 149981317 |
| Gene | SLC26A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs386833498 |
| dbSNP (classic) | rs386833498 |
| ClinGen | rs386833498 |
| ebi | rs386833498 |
| HLI | rs386833498 |
| Exac | rs386833498 |
| Gnomad | rs386833498 |
| Varsome | rs386833498 |
| LitVar | rs386833498 |
| Map | rs386833498 |
| PheGenI | rs386833498 |
| Biobank | rs386833498 |
| 1000 genomes | rs386833498 |
| hgdp | rs386833498 |
| ensembl | rs386833498 |
| geneview | rs386833498 |
| scholar | rs386833498 |
| rs386833498 | |
| pharmgkb | rs386833498 |
| gwascentral | rs386833498 |
| openSNP | rs386833498 |
| 23andMe | rs386833498 |
| SNPshot | rs386833498 |
| SNPdbe | rs386833498 |
| MSV3d | rs386833498 |
| GWAS Ctlg | rs386833498 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs386833498(-;-) |
| Alt | rs386833498(-;-) |
| Reference | Rs386833498(A;A) |
| Significance | Other |
| Disease | Diastrophic dysplasia Atelosteogenesis type 2 Achondrogenesis |
| Variation | info |
| Gene | SLC26A2 |
| CLNDBN | Diastrophic dysplasia Atelosteogenesis type 2 Achondrogenesis, type IB |
| Reversed | 0 |
| HGVS | NC_000005.9:g.149360880delA |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000004302.6, RCV000004303.4, RCV000023567.4, |
[PMID 7923357] The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.
[PMID 8702127] A family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans.
[PMID 8723100] A chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations.
