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rs36119840

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs36119840(A;A)
Make rs36119840(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position37816010
GeneGDNF
is asnp
is mentioned by
dbSNPrs36119840
ebirs36119840
HLIrs36119840
Exacrs36119840
Varsomers36119840
Maprs36119840
PheGenIrs36119840
hapmaprs36119840
1000 genomesrs36119840
hgdprs36119840
ensemblrs36119840
gopubmedrs36119840
geneviewrs36119840
scholarrs36119840
googlers36119840
pharmgkbrs36119840
gwascentralrs36119840
openSNPrs36119840
23andMers36119840
23andMe allrs36119840
SNP Nexus

SNPshotrs36119840
SNPdbers36119840
MSV3drs36119840
GWAS Ctlgrs36119840
Merged fromRs121918533
GMAF0.001837
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19184120] Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn

OMIM600837
Desc
Variant0001
Relatedalso


ClinVar
Risk rs36119840(A;A)
Alt rs36119840(A;A)
Reference rs36119840(G;G)
Significance Other
Disease Hirschsprung disease 3 Congenital central hypoventilation Pheochromocytoma not specified
Variation info
Gene GDNF
CLNDBN Hirschsprung disease 3 Congenital central hypoventilation Pheochromocytoma, modifier of not specified
Reversed 0
HGVS NC_000005.9:g.37816112G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009301.2, RCV000009302.3, RCV000009303.3, RCV000150719.1,