rs3208856
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3208856(C;C) |
Make rs3208856(C;T) |
Make rs3208856(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 19 |
Position | 44793549 |
Gene | CBLC |
is a | snp |
is | mentioned by |
dbSNP | rs3208856 |
dbSNP (classic) | rs3208856 |
ClinGen | rs3208856 |
ebi | rs3208856 |
HLI | rs3208856 |
Exac | rs3208856 |
Gnomad | rs3208856 |
Varsome | rs3208856 |
LitVar | rs3208856 |
Map | rs3208856 |
PheGenI | rs3208856 |
Biobank | rs3208856 |
1000 genomes | rs3208856 |
hgdp | rs3208856 |
ensembl | rs3208856 |
geneview | rs3208856 |
scholar | rs3208856 |
rs3208856 | |
pharmgkb | rs3208856 |
gwascentral | rs3208856 |
openSNP | rs3208856 |
23andMe | rs3208856 |
SNPshot | rs3208856 |
SNPdbe | rs3208856 |
MSV3d | rs3208856 |
GWAS Ctlg | rs3208856 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.