{{Rsnum
|rsid=80358228
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TACSTD2
|position=58576600
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TACSTD2
}}{{omim
|id=137290
|rsnum=80358228
|variant=0008
}}{{ClinVar
|rsid=80358228
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=58576600
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=TACSTD2:4070
|GENE_NAME=TACSTD2
|GENE_ID=4070
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.58576600A>G
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_002353.2:c.557T>C; 137290.0008
|CLNSIG=5
|CLNCUI=C0339273
|CLNDBN=Lattice corneal dystrophy Type III
|Disease=Lattice corneal dystrophy Type III
|CLNACC=RCV000017573.26
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=C0339273:204870:ORPHA98957:231928002:418946006
}}