{{Rsnum
|rsid=76466003
|Gene=GDNF
|Chromosome=5
|position=37815839
|Orientation=minus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GDNF
}}{{omim
|id=600837
|rsnum=76466003
|variant=0002
}}{{ClinVar
|rsid=76466003
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=37815941
|CHROM=5
|GMAF=0.0014
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=GDNF:2668
|GENE_NAME=GDNF
|GENE_ID=2668
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.37815941C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600837.0002
|CLNSIG=255
|CLNCUI=C2931739
|CLNDBN=Hirschsprung disease 3
|Disease=Hirschsprung disease 3
|CLNACC=RCV000009304.1
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1439:C2931739:613711:388
|COMMON=0
}}