{{Rsnum
|rsid=3026906
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ECE1
|position=21220008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ECE1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=600423
|rsnum=3026906
|variant=0001
}}

{{ClinVar
|rsid=3026906
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=21220008
|CHROM=1
|dbSNPBuildID=102
|SSR=0
|SAO=1
|VP=0x050260000a05000103110110
|GENEINFO=ECE1:1889
|GENE_NAME=ECE1
|GENE_ID=1889
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.21220008G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001113348.1:c.2212C>T; 600423.0001
|CLNSIG=5
|CLNCUI=C1838137
|CLNDBN=Hirschsprung disease, cardiac defects, and autonomic dysfunction
|Disease=Hirschsprung disease
|CLNACC=RCV000009704.3
|Tags=RV;PM;S3D;NSM;REF;ASP;GNO;OTHERKG;PH3;LSD;OM;NOC
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3151237:613870
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}