rs141374503
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs141374503(C;C) |
Make rs141374503(C;T) |
Make rs141374503(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 72313728 |
Gene | ADAMTS3 |
is a | snp |
is | mentioned by |
dbSNP | rs141374503 |
dbSNP (classic) | rs141374503 |
ClinGen | rs141374503 |
ebi | rs141374503 |
HLI | rs141374503 |
Exac | rs141374503 |
Gnomad | rs141374503 |
Varsome | rs141374503 |
LitVar | rs141374503 |
Map | rs141374503 |
PheGenI | rs141374503 |
Biobank | rs141374503 |
1000 genomes | rs141374503 |
hgdp | rs141374503 |
ensembl | rs141374503 |
geneview | rs141374503 |
scholar | rs141374503 |
rs141374503 | |
pharmgkb | rs141374503 |
gwascentral | rs141374503 |
openSNP | rs141374503 |
23andMe | rs141374503 |
SNPshot | rs141374503 |
SNPdbe | rs141374503 |
MSV3d | rs141374503 |
GWAS Ctlg | rs141374503 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.