Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730882219
rs730882219
Entrez Id: 50628
Gene Symbol: GEMIN4
GEMIN4
CUI: C4693567
Disease:
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES
G 0.800 CausalMutation CLINVAR
dbSNP: rs730882219
rs730882219
Entrez Id: 50628
Gene Symbol: GEMIN4
GEMIN4
CUI: C4693567
Disease:
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES
0.800 GeneticVariation UNIPROT