{{Rsnum
|rsid = 10456399
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Gene=TNXB
|Orientation=plus
|Chromosome=6
|position=31977789
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
}}{{Venter SNP
|rsid=10456399
|allele=G
|frequency=
|uid=1103652827645
|type=heterozygous_SNP
|hugo=TNXB
|ensembl gene=ENSG00000168477
|ensembl transcript=ENST00000299669
|sift=AFFECT FUNCTION
|disease=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
| rsid = 6457477
| distance = 398
}}
{{ neighbor
| rsid = 1135809
| distance = 209
}}