{{Rsnum
|rsid = 28941786
|Gene = CTH
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=1
|position=70430388
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CTH
}}{{omim
|desc=CYSTATHIONINURIA
|id=607657
|rsnum=28941786
|variant=0004
}}{{ClinVar
|rsid=28941786
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=70430388
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=CTH:1491
|GENE_NAME=CTH
|GENE_ID=1491
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.70430388C>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001902.5:c.718C>G; 607657.0004
|CLNSIG=5
|CLNCUI=C0220993
|CLNDBN=Cystathioninuria
|Disease=Cystathioninuria
|CLNACC=RCV000003074.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0220993:219500:ORPHA212:13003007
}}

{{on chip | 23andMe v4}}