rs201226914
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs201226914(G;G) |
Make rs201226914(G;T) |
Make rs201226914(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 88732511 |
Gene | LOC100289580, PIEZO1 |
is a | snp |
is | mentioned by |
dbSNP | rs201226914 |
dbSNP (classic) | rs201226914 |
ClinGen | rs201226914 |
ebi | rs201226914 |
HLI | rs201226914 |
Exac | rs201226914 |
Gnomad | rs201226914 |
Varsome | rs201226914 |
LitVar | rs201226914 |
Map | rs201226914 |
PheGenI | rs201226914 |
Biobank | rs201226914 |
1000 genomes | rs201226914 |
hgdp | rs201226914 |
ensembl | rs201226914 |
geneview | rs201226914 |
scholar | rs201226914 |
rs201226914 | |
pharmgkb | rs201226914 |
gwascentral | rs201226914 |
openSNP | rs201226914 |
23andMe | rs201226914 |
SNPshot | rs201226914 |
SNPdbe | rs201226914 |
MSV3d | rs201226914 |
GWAS Ctlg | rs201226914 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.