{{Rsnum
|rsid=11570255
|Gene=EDN3
|Chromosome=20
|position=59300861
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.00551
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=EDN3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 9.2 | 90.8
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.9 | 3.8 | 95.3
| GIH | 0.0 | 11.2 | 88.8
| LWK | 0.0 | 1.0 | 99.0
| MEX | 0.0 | 7.1 | 92.9
| MKK | 0.0 | 0.7 | 99.3
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=HIRSCHSPRUNG DISEASE
|id=131242
|rsnum=11570255
|variant=0004
}}

{{ClinVar
|rsid=11570255
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=57875916
|CHROM=20
|GMAF=0.0055
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050060000000040517110100
|GENEINFO=EDN3:1908
|GENE_NAME=EDN3
|GENE_ID=1908
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.57875916G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=131242.0004
|CLNSIG=255
|CLNCUI=C3150975
|CLNDBN=Hirschsprung disease 4
|Disease=Hirschsprung disease 4
|CLNACC=RCV000018126.1
|Tags=PM;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9945; 0.00551
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3150975:613712:388
|COMMON=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}