rs1616905
From SNPedia
Merged into | rs828199 |
Orientation | plus |
Stabilized | plus |
Make rs1616905(C;C) |
Make rs1616905(C;T) |
Make rs1616905(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 90718584 |
is a | snp |
is | mentioned by |
dbSNP | rs1616905 |
dbSNP (classic) | rs1616905 |
ClinGen | rs1616905 |
ebi | rs1616905 |
HLI | rs1616905 |
Exac | rs1616905 |
Gnomad | rs1616905 |
Varsome | rs1616905 |
LitVar | rs1616905 |
Map | rs1616905 |
PheGenI | rs1616905 |
Biobank | rs1616905 |
1000 genomes | rs1616905 |
hgdp | rs1616905 |
ensembl | rs1616905 |
geneview | rs1616905 |
scholar | rs1616905 |
rs1616905 | |
pharmgkb | rs1616905 |
gwascentral | rs1616905 |
openSNP | rs1616905 |
23andMe | rs1616905 |
SNPshot | rs1616905 |
SNPdbe | rs1616905 |
MSV3d | rs1616905 |
GWAS Ctlg | rs1616905 |
Status | Merged into rs828199 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20863575] Lack of association between response of OROS-methylphenidate and norepinephrine transporter (SLC6A2) polymorphism in Korean ADHD