rs1009316
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1009316(C;C) |
Make rs1009316(C;T) |
Make rs1009316(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 48955313 |
Gene | BAX |
is a | snp |
is | mentioned by |
dbSNP | rs1009316 |
dbSNP (classic) | rs1009316 |
ClinGen | rs1009316 |
ebi | rs1009316 |
HLI | rs1009316 |
Exac | rs1009316 |
Gnomad | rs1009316 |
Varsome | rs1009316 |
LitVar | rs1009316 |
Map | rs1009316 |
PheGenI | rs1009316 |
Biobank | rs1009316 |
1000 genomes | rs1009316 |
hgdp | rs1009316 |
ensembl | rs1009316 |
geneview | rs1009316 |
scholar | rs1009316 |
rs1009316 | |
pharmgkb | rs1009316 |
gwascentral | rs1009316 |
openSNP | rs1009316 |
23andMe | rs1009316 |
SNPshot | rs1009316 |
SNPdbe | rs1009316 |
MSV3d | rs1009316 |
GWAS Ctlg | rs1009316 |
GMAF | 0.1644 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24474449] Association between SNPs in P53 binding regions and risk of esophageal squamous cell carcinoma