{{Rsnum
|rsid=36119840
|Gene=GDNF
|Chromosome=5
|position=37816010
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GDNF
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 1.8 | 98.2
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 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 | 1.0 | 99.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19184120
|Title=Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn
}}

{{omim
|id=600837
|rsnum=36119840
|variant=0001
}}

{{ClinVar
|rsid=36119840
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=37816112
|CHROM=5
|GMAF=0.0018
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x05036800000004051f110100
|GENEINFO=GDNF:2668
|GENE_NAME=GDNF
|GENE_ID=2668
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.37816112G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600837.0001
|CLNSIG=255
|CLNCUI=C2931739; C1859049
|CLNDBN=Hirschsprung disease 3; Congenital central hypoventilation; Pheochromocytoma, modifier of
|Disease=Hirschsprung disease 3; Congenital central hypoventilation; Pheochromocytoma
|CLNACC=RCV000009301.1; RCV000009302.2; RCV000009303.1
|Tags=PM;PMC;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1439:C2931739:613711:388; NBK1427:C1859049:209880:661:99803:399040002
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}