rs554375713
From SNPedia
Merged into | rs587776842 |
Orientation | plus |
Make rs554375713(-;-) |
Make rs554375713(-;CCGCCGACCTCCT) |
Make rs554375713(CCGCCGACCTCCT;CCGCCGACCTCCT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 637537 |
Gene | DRD4 |
is a | snp |
is | mentioned by |
dbSNP | rs554375713 |
dbSNP (classic) | rs554375713 |
ClinGen | rs554375713 |
ebi | rs554375713 |
HLI | rs554375713 |
Exac | rs554375713 |
Gnomad | rs554375713 |
Varsome | rs554375713 |
LitVar | rs554375713 |
Map | rs554375713 |
PheGenI | rs554375713 |
Biobank | rs554375713 |
1000 genomes | rs554375713 |
hgdp | rs554375713 |
ensembl | rs554375713 |
geneview | rs554375713 |
scholar | rs554375713 |
rs554375713 | |
pharmgkb | rs554375713 |
gwascentral | rs554375713 |
openSNP | rs554375713 |
23andMe | rs554375713 |
SNPshot | rs554375713 |
SNPdbe | rs554375713 |
MSV3d | rs554375713 |
GWAS Ctlg | rs554375713 |
Status | Merged into rs587776842 |
Max Magnitude | 0 |
rs554375713 designates a variant consisting of a 13-bp deletion of bases 235 to 247 in exon 1 of the DRD4 gene on chromosome 11.