rs6054906
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6054906(A;A) |
Make rs6054906(A;G) |
Make rs6054906(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 7314256 |
is a | snp |
is | mentioned by |
dbSNP | rs6054906 |
dbSNP (classic) | rs6054906 |
ClinGen | rs6054906 |
ebi | rs6054906 |
HLI | rs6054906 |
Exac | rs6054906 |
Gnomad | rs6054906 |
Varsome | rs6054906 |
LitVar | rs6054906 |
Map | rs6054906 |
PheGenI | rs6054906 |
Biobank | rs6054906 |
1000 genomes | rs6054906 |
hgdp | rs6054906 |
ensembl | rs6054906 |
geneview | rs6054906 |
scholar | rs6054906 |
rs6054906 | |
pharmgkb | rs6054906 |
gwascentral | rs6054906 |
openSNP | rs6054906 |
23andMe | rs6054906 |
SNPshot | rs6054906 |
SNPdbe | rs6054906 |
MSV3d | rs6054906 |
GWAS Ctlg | rs6054906 |
GMAF | 0.4435 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22952603![]() |
Trait | Response to amphetamines |
Title | Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13). |
Risk Allele | |
P-val | 3E-6 |
Odds Ratio | NR NR |
[PMID 17186469] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.