rs28925904
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs28925904(C;C) |
Make rs28925904(C;T) |
Make rs28925904(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 143438337 |
Gene | GAB1 |
is a | snp |
is | mentioned by |
dbSNP | rs28925904 |
dbSNP (classic) | rs28925904 |
ClinGen | rs28925904 |
ebi | rs28925904 |
HLI | rs28925904 |
Exac | rs28925904 |
Gnomad | rs28925904 |
Varsome | rs28925904 |
LitVar | rs28925904 |
Map | rs28925904 |
PheGenI | rs28925904 |
Biobank | rs28925904 |
1000 genomes | rs28925904 |
hgdp | rs28925904 |
ensembl | rs28925904 |
geneview | rs28925904 |
scholar | rs28925904 |
rs28925904 | |
pharmgkb | rs28925904 |
gwascentral | rs28925904 |
openSNP | rs28925904 |
23andMe | rs28925904 |
SNPshot | rs28925904 |
SNPdbe | rs28925904 |
MSV3d | rs28925904 |
GWAS Ctlg | rs28925904 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.