{{Rsnum
|rsid=104893891
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=GDNF
|position=37815827
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GDNF
}}{{omim
|id=600837
|rsnum=104893891
|variant=0003
}}{{ClinVar
|rsid=104893891
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=37815929
|CHROM=5
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GDNF:2668
|GENE_NAME=GDNF
|GENE_ID=2668
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.37815929T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600837.0003
|CLNSIG=255
|CLNCUI=C2931739
|CLNDBN=Hirschsprung disease 3
|Disease=Hirschsprung disease 3
|CLNACC=RCV000009305.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1439:C2931739:613711:388
}}