{{Rsnum
|rsid=57872071
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KRT3
|position=52791216
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT3
}}{{omim
|id=148043
|rsnum=57872071
|variant=0001
}}

{{ClinVar
|rsid=57872071
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=53185000
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT3:3850
|GENE_NAME=KRT3
|GENE_ID=3850
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.53185000C>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT3:c.1525G>A; 148043.0001
|CLNSIG=5
|CLNCUI=C0339277
|CLNDBN=Meesman's corneal dystrophy; not provided
|Disease=Meesman's corneal dystrophy; not provided
|CLNACC=RCV000015738.24; RCV000057204.1
|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}}