rs730882220, FAM20C

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neonatal Death
CUI: C0410916
Disease: Neonatal Death
0.700 GeneticVariation CLINVAR
Cortical Dysplasia
CUI: C0431380
Disease: Cortical Dysplasia
0.700 GeneticVariation CLINVAR
Dysmorphic facies
CUI: C0424503
Disease: Dysmorphic facies
0.700 GeneticVariation CLINVAR