Disease: MECKEL SYNDROME, TYPE 6 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386833747
rs386833747
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C2676790
Disease:
MECKEL SYNDROME, TYPE 6 (disorder) 		C 0.700 GeneticVariation CLINVAR