Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205664
rs786205664
Entrez Id: 128338
Gene Symbol: DRAM2
DRAM2
CUI: C4049066
Disease:
Retinal dystrophy with early macular involvement
A 0.800 CausalMutation CLINVAR
dbSNP: rs786205664
rs786205664
Entrez Id: 128338
Gene Symbol: DRAM2
DRAM2
CUI: C4049066
Disease:
Retinal dystrophy with early macular involvement
0.800 GeneticVariation UNIPROT