Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553827236
rs1553827236
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C0426790
Disease:
Narrow thorax
A 0.700 CausalMutation CLINVAR