rs121918536
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs121918536(C;G) |
Make rs121918536(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 37815654 |
Gene | GDNF |
is a | snp |
is | mentioned by |
dbSNP | rs121918536 |
dbSNP (classic) | rs121918536 |
ClinGen | rs121918536 |
ebi | rs121918536 |
HLI | rs121918536 |
Exac | rs121918536 |
Gnomad | rs121918536 |
Varsome | rs121918536 |
LitVar | rs121918536 |
Map | rs121918536 |
PheGenI | rs121918536 |
Biobank | rs121918536 |
1000 genomes | rs121918536 |
hgdp | rs121918536 |
ensembl | rs121918536 |
geneview | rs121918536 |
scholar | rs121918536 |
rs121918536 | |
pharmgkb | rs121918536 |
gwascentral | rs121918536 |
openSNP | rs121918536 |
23andMe | rs121918536 |
SNPshot | rs121918536 |
SNPdbe | rs121918536 |
MSV3d | rs121918536 |
GWAS Ctlg | rs121918536 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121918536(G;G) |
Alt | rs121918536(G;G) |
Reference | Rs121918536(C;C) |
Significance | Other |
Disease | Hirschsprung disease 3 |
Variation | info |
Gene | GDNF |
CLNDBN | Hirschsprung disease 3 |
Reversed | 1 |
HGVS | NC_000005.9:g.37815756G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000009306.3, |