{{Rsnum
|rsid=104894704
|Gene=KLK4
|Chromosome=19
|position=50908596
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KLK4
}}{{omim
|id=603767
|rsnum=104894704
|variant=0001
}}{{ClinVar
|rsid=104894704
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=51411852
|CHROM=19
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=KLK4:9622
|GENE_NAME=KLK4
|GENE_ID=9622
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.51411852C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNACC=RCV000006452.1
|CLNDBN=Amelogenesis imperfecta pigmented hypomaturation type
|CLNDSDB=MedGen
|CLNDSDBID=C1290537
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603767.0001
|COMMON=1
|Disease=Amelogenesis imperfecta pigmented hypomaturation type
}}