Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199584830
rs199584830
Entrez Id: 1259;152519;101927157
Gene Symbol: CNGA1;NIPAL1;LOC101927157
CNGA1;NIPAL1;LOC101927157
CUI: C0854723
Disease:
Retinal Dystrophies
A 0.700 GeneticVariation CLINVAR