Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142110773
rs142110773
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C0026351
Disease:
Moderate intellectual disability
A 0.700 GeneticVariation CLINVAR