Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs151340626
rs151340626
Entrez Id: 1184
Gene Symbol: CLCN5
CLCN5
CUI: C0878681
Disease:
Dent's disease
0.710 GeneticVariation BEFREE CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets. 9452997 1998
dbSNP: rs151340626
rs151340626
Entrez Id: 1184
Gene Symbol: CLCN5
CLCN5
CUI: C0878681
Disease:
Dent's disease
T 0.710 CausalMutation CLINVAR