rs34471628
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs34471628(C;C) |
Make rs34471628(C;T) |
Make rs34471628(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 172769749 |
Gene | DUSP1 |
is a | snp |
is | mentioned by |
dbSNP | rs34471628 |
dbSNP (classic) | rs34471628 |
ClinGen | rs34471628 |
ebi | rs34471628 |
HLI | rs34471628 |
Exac | rs34471628 |
Gnomad | rs34471628 |
Varsome | rs34471628 |
LitVar | rs34471628 |
Map | rs34471628 |
PheGenI | rs34471628 |
Biobank | rs34471628 |
1000 genomes | rs34471628 |
hgdp | rs34471628 |
ensembl | rs34471628 |
geneview | rs34471628 |
scholar | rs34471628 |
rs34471628 | |
pharmgkb | rs34471628 |
gwascentral | rs34471628 |
openSNP | rs34471628 |
23andMe | rs34471628 |
SNPshot | rs34471628 |
SNPdbe | rs34471628 |
MSV3d | rs34471628 |
GWAS Ctlg | rs34471628 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.