Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555302200
rs1555302200
Entrez Id: 57096
Gene Symbol: RPGRIP1
RPGRIP1
CUI: C0271385
Disease:
Horizontal Nystagmus
CTT 0.700 GeneticVariation CLINVAR