Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
0.710 GeneticVariation BEFREE We detected two distinct mutations, p.T7FX7 (c.18-21del4bp) and p.E227E (c.681 G>A) (homozygous), in the CTNS gene in 11 patients with cystinosis from the East Anatolian region of Turkey. 27269891 2016
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
G 0.710 CausalMutation CLINVAR Genetic basis of cystinosis in Turkish patients: a single-center experience. 21786142 2012
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
G 0.710 CausalMutation CLINVAR Analysis of the CTNS gene in 32 cystinosis patients from Spain. 19863563 2009
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
G 0.710 CausalMutation CLINVAR Analysis of the CTNS gene in patients of German and Swiss origin with nephropathic cystinosis. 12204010 2002
dbSNP: rs113994205
rs113994205
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
0.710 GeneticVariation BEFREE According to a cystinosis clinical severity score, homozygotes for the 65-kb deletion and for W138X have average disease, whereas mutations involving the first amino acids prior to transmembrane domains are associated with mild disease. 9792862 1998
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
G 0.710 CausalMutation CLINVAR CTNS mutations in an American-based population of cystinosis patients. 9792862 1998
dbSNP: rs786204501
rs786204501
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
G 0.710 CausalMutation CLINVAR A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. 9537412 1998
dbSNP: rs113994205
rs113994205
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
A 0.710 CausalMutation CLINVAR
dbSNP: rs113994204
rs113994204
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
A 0.700 CausalMutation CLINVAR Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. 26489029 2016
dbSNP: rs786204420
rs786204420
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
CG 0.700 CausalMutation CLINVAR Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier Screening. 27533158 2016
dbSNP: rs759623796
rs759623796
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 CausalMutation CLINVAR Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene. 26266097 2015
dbSNP: rs786204632
rs786204632
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic Cystinosis. 24464559 2014
dbSNP: rs550254092
rs550254092
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR CTNS gene analysis emphasizes diagnostic value of eye examination in patients with cystinosis. 27625850 2013
dbSNP: rs113994208
rs113994208
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
A 0.700 CausalMutation CLINVAR A co-occurrence of osteogenesis imperfecta type VI and cystinosis. 22528245 2012
dbSNP: rs113994208
rs113994208
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
A 0.700 CausalMutation CLINVAR Mechanism of proton/substrate coupling in the heptahelical lysosomal transporter cystinosin. 22232659 2012
dbSNP: rs786204420
rs786204420
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
CG 0.700 CausalMutation CLINVAR Detailed studies of growth hormone secretion in cystinosis patients. 22664570 2012
dbSNP: rs113994204
rs113994204
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
A 0.700 GeneticVariation CLINVAR Non-invasive measurements of atherosclerosis in adult cystinosis patients. 21305353 2011
dbSNP: rs786204550
rs786204550
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR Non-invasive measurements of atherosclerosis in adult cystinosis patients. 21305353 2011
dbSNP: rs267606754
rs267606754
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR Analysis of the CTNS gene in 32 cystinosis patients from Spain. 19863563 2009
dbSNP: rs786204632
rs786204632
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR An Indian boy with nephropathic cystinosis: a case report and molecular analysis of CTNS mutation. 19580442 2009
dbSNP: rs113994204
rs113994204
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
A 0.700 CausalMutation CLINVAR Analysis of the CTNS gene in nephropathic cystinosis Mexican patients: report of four novel mutations and identification of a false positive 57-kb deletion genotype with LDM-2/exon 4 multiplex PCR assay. 18752449 2008
dbSNP: rs113994204
rs113994204
Entrez Id: 1497;105371493
Gene Symbol: CTNS;LOC105371493
CTNS;LOC105371493
CUI: C4316899
Disease:
Cystinosis
A 0.700 GeneticVariation CLINVAR Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin. 15128704 2004
dbSNP: rs113994208
rs113994208
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
A 0.700 CausalMutation CLINVAR Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin. 15128704 2004
dbSNP: rs267606754
rs267606754
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
T 0.700 GeneticVariation CLINVAR Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin. 15128704 2004
dbSNP: rs760256854
rs760256854
Entrez Id: 1497;105371492
Gene Symbol: CTNS;LOC105371492
CTNS;LOC105371492
CUI: C4316899
Disease:
Cystinosis
A 0.700 GeneticVariation CLINVAR Molecular pathogenesis of cystinosis: effect of CTNS mutations on the transport activity and subcellular localization of cystinosin. 15128704 2004