{{Rsnum
|rsid = 36007903
|Status = Merged
|Merged = 4959084
|Gene=TNXA
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=6
|position=31976926
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}{{Venter SNP
|rsid=36007903
|allele=T
|frequency=
|uid=1103652827631
|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 = 35445429
| distance = 10
}}
{{ neighbor
| rsid = 6941704
| distance = 241
}}