{{Rsnum
|rsid=35086888
|Gene=CTNS
|Chromosome=17
|position=3647506
|Orientation=plus
|GMAF=0.01607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CTNS
}}{{omim
|id=606272
|rsnum=35086888
|variant=0007
}}

{{ClinVar
|rsid=35086888
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=3550800
|CHROM=17
|GMAF=0.016
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050060000000150516110100
|GENEINFO=CTNS:1497
|GENE_NAME=CTNS
|GENE_ID=1497
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.3550800G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9839; 0.01607
|CLNACC=RCV000004700.1
|CLNDBN=Cystinosis, atypical nephropathic
|CLNDSDB=MedGen
|CLNDSDBID=C2749685
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606272.0007
|COMMON=1
|Disease=Cystinosis
}}

{{GET Evidence
|gene=CTNS
|aa_change=Val42Ile
|aa_change_short=V42I
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs35086888
|overall_frequency_n=197
|overall_frequency_d=10758
|overall_frequency=0.018312
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=1
|n_articles_annotated=1
|gene_in_genetests=Y
|in_omim=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-4
|autoscore=5
|webscore=N
|n_web_uneval=3
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}