Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1558192351
rs1558192351
Entrez Id: 9095
Gene Symbol: TBX19
TBX19
CUI: C0271583
Disease:
ACTH Deficiency, Isolated
A 0.700 CausalMutation CLINVAR