{{Rsnum
|rsid=57218384
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KRT12
|position=39023035
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=601687
|rsnum=57218384
|variant=0001
}}
{{omim
|id=601687
|rsnum=57218384
|variant=0004
}}

{{ClinVar
|rsid=57218384
|Reversed=1
|FwdREF=G
|FwdALT=C,T
|REF=C
|ALT=A,G
|RSPOS=39023035
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT12:3859
|GENE_NAME=KRT12
|GENE_ID=3859
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.39023035C>A; NC_000017.10:g.39023035C>G
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT12:c.404G>T; 601687.0004; KRT12:c.404G>C; 601687.0001
|CLNSIG=5
|CLNCUI=C0339277
|CLNDBN=Meesman's corneal dystrophy; not provided
|Disease=Meesman's corneal dystrophy; not provided
|CLNACC=RCV000008386.1; RCV000056422.1; RCV000008383.1; RCV000056421.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0339277:122100:98954:1674008
}}

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