Rs6457477
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs6457477 |
| hapmap | rs6457477 |
| hgdp | rs6457477 |
| ensembl | rs6457477 |
| gopubmed | rs6457477 |
| scholar | rs6457477 |
| rs6457477 | |
| pharmgkb | rs6457477 |
| hgvbaseg2p | rs6457477 |
| medrefsnp | rs6457477 |
| 23andMe | rs6457477 |
| SNP Nexus |
| Gene | TNXB |
| Chromosome | 6 |
| Orientation | plus |
| Position | 32085368 |
| Genotype | Effect |
|---|---|
| rs6457477(C;C)* | ? |
| rs6457477(C;T)* | ? |
| rs6457477(T;T)* | ? |
| Venter snp | |
|---|---|
| Source | plos |
| Gene | TNXB |
| allele | T |
| frequency | |
| sift | AFFECT FUNCTION |
| HuRef | 1103652827635 |
| Disease Association | Defects in TNXB are the cause of Ehlers-Danlos-like syndrome (MIM:606408). This clinically distinct form of Ehlers- Danlos syndrome is characterized by hyperextensible skin, hypermobile joints, and tissue fragility, but it lacks atrophic scars and delayed wound healing. Inheritance is autosomal recessive. |
| Neighbor | rs6941704 |
| Distance | 224 |
| Neighbor | rs10456399 |
| Distance | 398 |