{{Rsnum
|rsid = 1135809
|Gene=TNXA
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=6
|position=31977998
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}{{Venter SNP
|rsid=1135809
|allele=G
|frequency=
|uid=1103652827646
|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 = 10456399
| distance = 209
}}