{{Rsnum
|rsid=74315384
|Chromosome=20
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=EDN3
|position=59321127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EDN3
}}{{omim
|id=131242
|rsnum=74315384
|variant=0002
}}{{ClinVar
|rsid=74315384
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=57896182
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=EDN3:1908
|GENE_NAME=EDN3
|GENE_ID=1908
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.57896182G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=131242.0002
|CLNSIG=5
|CLNCUI=C2750457
|CLNDBN=Waardenburg syndrome type 4B
|Disease=Waardenburg syndrome type 4B
|CLNACC=RCV000018124.26
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2750457:613265:897
}}