rs3837091
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AGAG;AGAG) | 0 | common in clinvar |
Make rs3837091(-;-) |
Make rs3837091(-;GAGA) |
Make rs3837091(GAGA;GAGA) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 50561043 |
Gene | DDC |
is a | snp |
is | mentioned by |
dbSNP | rs3837091 |
dbSNP (classic) | rs3837091 |
ClinGen | rs3837091 |
ebi | rs3837091 |
HLI | rs3837091 |
Exac | rs3837091 |
Gnomad | rs3837091 |
Varsome | rs3837091 |
LitVar | rs3837091 |
Map | rs3837091 |
PheGenI | rs3837091 |
Biobank | rs3837091 |
1000 genomes | rs3837091 |
hgdp | rs3837091 |
ensembl | rs3837091 |
geneview | rs3837091 |
scholar | rs3837091 |
rs3837091 | |
pharmgkb | rs3837091 |
gwascentral | rs3837091 |
openSNP | rs3837091 |
23andMe | rs3837091 |
SNPshot | rs3837091 |
SNPdbe | rs3837091 |
MSV3d | rs3837091 |
GWAS Ctlg | rs3837091 |
Max Magnitude | 0 |
[PMID 25805645] Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease
ClinVar | |
---|---|
Risk | rs3837091(GAGA;GAGA) rs3837091(CTCT;CTCT) rs3837091(-;-) |
Alt | rs3837091(GAGA;GAGA) rs3837091(CTCT;CTCT) rs3837091(-;-) |
Reference | Rs3837091(AGAG;AGAG) |
Significance | Non-pathogenic |
Disease | Deficiency of aromatic-L-amino-acid decarboxylase |
Variation | info |
Gene | DDC |
CLNDBN | Deficiency of aromatic-L-amino-acid decarboxylase |
Reversed | 1 |
HGVS | NC_000007.13:g.50628740_50628743delCTCT |
CLNSRC | |
CLNACC | RCV000369935.1, |