{{Rsnum
|rsid=121908426
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EVC
|position=5745321
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EVC
}}{{omim
|id=604831
|rsnum=121908426
|variant=0006
}}{{ClinVar
|rsid=121908426
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=5747048
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=EVC:2121
|GENE_NAME=EVC
|GENE_ID=2121
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.5747048T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604831.0006
|CLNSIG=5
|CLNCUI=C0457013; C0013903
|CLNDBN=Curry-Hall syndrome; Chondroectodermal dysplasia
|Disease=Curry-Hall syndrome; Chondroectodermal dysplasia
|CLNACC=RCV000005671.1; RCV000005672.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0457013:193530:952:277807007; C0013903:225500:289:62501005
}}