{{Rsnum
|rsid=1801710
|Gene=EDNRB
|Chromosome=13
|position=77918405
|Orientation=minus
|GMAF=0.004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=EDNRB
}}{{omim
|id=131244
|rsnum=1801710
|variant=0005
}}{{ClinVar
|rsid=1801710
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=78492540
|CHROM=13
|GMAF=0.0046
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050060000000050516110100
|GENEINFO=EDNRB:1910
|GENE_NAME=EDNRB
|GENE_ID=1910
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.78492540C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=131244.0005
|CLNSIG=255
|CLNCUI=C1838564
|CLNDBN=Hirschsprung disease 2
|Disease=Hirschsprung disease 2
|CLNACC=RCV000018117.1
|Tags=RV;PM;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9954; 0.004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1439:C1838564:600155:388
|COMMON=1
}}