rs147110934
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147110934(G;G) |
Make rs147110934(G;T) |
Make rs147110934(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 19 |
Position | 55482069 |
Gene | ZNF628 |
is a | snp |
is | mentioned by |
dbSNP | rs147110934 |
dbSNP (classic) | rs147110934 |
ClinGen | rs147110934 |
ebi | rs147110934 |
HLI | rs147110934 |
Exac | rs147110934 |
Gnomad | rs147110934 |
Varsome | rs147110934 |
LitVar | rs147110934 |
Map | rs147110934 |
PheGenI | rs147110934 |
Biobank | rs147110934 |
1000 genomes | rs147110934 |
hgdp | rs147110934 |
ensembl | rs147110934 |
geneview | rs147110934 |
scholar | rs147110934 |
rs147110934 | |
pharmgkb | rs147110934 |
gwascentral | rs147110934 |
openSNP | rs147110934 |
23andMe | rs147110934 |
SNPshot | rs147110934 |
SNPdbe | rs147110934 |
MSV3d | rs147110934 |
GWAS Ctlg | rs147110934 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.