Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs368720062
rs368720062
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C0265215
Disease:
Meckel-Gruber syndrome
C 0.700 GeneticVariation CLINVAR