Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201620629
rs201620629
TBX6
A 0.700 CausalMutation CLINVAR TBX6 null variants and a common hypomorphic allele in congenital scoliosis. 25564734

2015
dbSNP: rs201620629
rs201620629
TBX6
A 0.700 CausalMutation CLINVAR Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. 23335591

2013