Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202193096
rs202193096
TBX6
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		A 0.700 GeneticVariation CLINVAR TBX6 null variants and a common hypomorphic allele in congenital scoliosis. 25564734

2015