Rs10456399
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10456399 |
| hapmap | rs10456399 |
| hgdp | rs10456399 |
| ensembl | rs10456399 |
| gopubmed | rs10456399 |
| scholar | rs10456399 |
| rs10456399 | |
| pharmgkb | rs10456399 |
| hgvbaseg2p | rs10456399 |
| medrefsnp | rs10456399 |
| 23andMe | rs10456399 |
| SNP Nexus |
| Gene | TNXB |
| Chromosome | 6 |
| Orientation | plus |
| Position | 32085766 |
| Genotype | Effect |
|---|---|
| rs10456399(A;A)* | ? |
| rs10456399(A;G)* | ? |
| rs10456399(G;G)* | ? |
| Venter snp | |
|---|---|
| Source | plos |
| Gene | TNXB |
| allele | G |
| frequency | |
| sift | AFFECT FUNCTION |
| HuRef | 1103652827645 |
| 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 | rs6457477 |
| Distance | 398 |
| Neighbor | rs1135809 |
| Distance | 209 |