Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28928903
rs28928903
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
0.800 GeneticVariation UNIPROT

dbSNP: rs28928903
rs28928903
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
C 0.800 CausalMutation CLINVAR