rs116807401
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs116807401(C;C) |
Make rs116807401(C;T) |
Make rs116807401(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 134200566 |
Gene | PABPC4L |
is a | snp |
is | mentioned by |
dbSNP | rs116807401 |
dbSNP (classic) | rs116807401 |
ClinGen | rs116807401 |
ebi | rs116807401 |
HLI | rs116807401 |
Exac | rs116807401 |
Gnomad | rs116807401 |
Varsome | rs116807401 |
LitVar | rs116807401 |
Map | rs116807401 |
PheGenI | rs116807401 |
Biobank | rs116807401 |
1000 genomes | rs116807401 |
hgdp | rs116807401 |
ensembl | rs116807401 |
geneview | rs116807401 |
scholar | rs116807401 |
rs116807401 | |
pharmgkb | rs116807401 |
gwascentral | rs116807401 |
openSNP | rs116807401 |
23andMe | rs116807401 |
SNPshot | rs116807401 |
SNPdbe | rs116807401 |
MSV3d | rs116807401 |
GWAS Ctlg | rs116807401 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.