rs6948
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs6948(A;A) |
Make rs6948(A;C) |
Make rs6948(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 184627976 |
Gene | CASP3 |
is a | snp |
is | mentioned by |
dbSNP | rs6948 |
dbSNP (classic) | rs6948 |
ClinGen | rs6948 |
ebi | rs6948 |
HLI | rs6948 |
Exac | rs6948 |
Gnomad | rs6948 |
Varsome | rs6948 |
LitVar | rs6948 |
Map | rs6948 |
PheGenI | rs6948 |
Biobank | rs6948 |
1000 genomes | rs6948 |
hgdp | rs6948 |
ensembl | rs6948 |
geneview | rs6948 |
scholar | rs6948 |
rs6948 | |
pharmgkb | rs6948 |
gwascentral | rs6948 |
openSNP | rs6948 |
23andMe | rs6948 |
SNPshot | rs6948 |
SNPdbe | rs6948 |
MSV3d | rs6948 |
GWAS Ctlg | rs6948 |
GMAF | 0.4412 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22568453] Association of CASP3 polymorphism with hematologic toxicity in advanced NSCLC patients treated with platinum-based chemotherapy
[PMID 17071630] Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma.
[PMID 18381704] Caspase polymorphisms and genetic susceptibility to multiple myeloma.
[PMID 18829519] CASP3 polymorphisms and risk of squamous cell carcinoma of the head and neck.
[PMID 28738811] Associations of genetic variation in CASP3 gene with noise-induced hearing loss in a Chinese population: a case-control study.