rs36119840
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs36119840(A;A) |
Make rs36119840(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 37816010 |
Gene | GDNF |
is a | snp |
is | mentioned by |
dbSNP | rs36119840 |
dbSNP (classic) | rs36119840 |
ClinGen | rs36119840 |
ebi | rs36119840 |
HLI | rs36119840 |
Exac | rs36119840 |
Gnomad | rs36119840 |
Varsome | rs36119840 |
LitVar | rs36119840 |
Map | rs36119840 |
PheGenI | rs36119840 |
Biobank | rs36119840 |
1000 genomes | rs36119840 |
hgdp | rs36119840 |
ensembl | rs36119840 |
geneview | rs36119840 |
scholar | rs36119840 |
rs36119840 | |
pharmgkb | rs36119840 |
gwascentral | rs36119840 |
openSNP | rs36119840 |
23andMe | rs36119840 |
SNPshot | rs36119840 |
SNPdbe | rs36119840 |
MSV3d | rs36119840 |
GWAS Ctlg | rs36119840 |
Merged from | Rs121918533 |
GMAF | 0.001837 |
Max Magnitude | 0 |
? | (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
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 UniProtKB (protein) |
CLNACC | RCV000009301.2, RCV000009302.3, RCV000009303.3, RCV000150719.1, |