{{Rsnum
|rsid=104894391
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=EDNRB
|position=77903356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EDNRB,SLFN14
}}{{omim
|id=131244
|rsnum=104894391
|variant=0008
}}{{ClinVar
|rsid=104894391
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=78477491
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=EDNRB:1910; EDNRB-AS1:100505518
|GENE_NAME=EDNRB; EDNRB-AS1
|GENE_ID=1910; 100505518
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.78477491G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=131244.0008
|CLNSIG=5
|CLNCUI=C1838099
|CLNDBN=ABCD syndrome
|Disease=ABCD syndrome
|CLNACC=RCV000018120.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838099:600501
}}