{{Rsnum
|rsid=28941785
|Gene=CTH
|Chromosome=1
|position=70415987
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.003214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CTH
}}{{omim
|desc=CYSTATHIONINURIA
|id=607657
|rsnum=28941785
|variant=0003
}}

{{ClinVar
|rsid=28941785
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=70415987
|CHROM=1
|GMAF=0.0032
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050260400a05040416110100
|GENEINFO=CTH:1491
|GENE_NAME=CTH
|GENE_ID=1491
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.70415987C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001902.5:c.200C>T; 607657.0003
|CLNSIG=5
|CLNCUI=C0220993
|CLNDBN=Cystathioninuria
|Disease=Cystathioninuria
|CLNACC=RCV000003073.1
|Tags=PM;S3D;NSM;REF;U5;ASP;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0220993:219500:ORPHA212:13003007
|COMMON=1
}}

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