{{Rsnum
|rsid = 6941704
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Gene=TNXA
|Orientation=plus
|Chromosome=6
|position=32042125
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2,TNXB
}}{{Venter SNP
|rsid=6941704
|allele=T
|frequency=
|uid=1103652827632
|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 = 36007903
| distance = 241
}}
{{ neighbor
| rsid = 6457477
| distance = 224
}}