rs2020902
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs2020902(C;C) |
Make rs2020902(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 15507865 |
Gene | CASP9 |
is a | snp |
is | mentioned by |
dbSNP | rs2020902 |
dbSNP (classic) | rs2020902 |
ClinGen | rs2020902 |
ebi | rs2020902 |
HLI | rs2020902 |
Exac | rs2020902 |
Gnomad | rs2020902 |
Varsome | rs2020902 |
LitVar | rs2020902 |
Map | rs2020902 |
PheGenI | rs2020902 |
Biobank | rs2020902 |
1000 genomes | rs2020902 |
hgdp | rs2020902 |
ensembl | rs2020902 |
geneview | rs2020902 |
scholar | rs2020902 |
rs2020902 | |
pharmgkb | rs2020902 |
gwascentral | rs2020902 |
openSNP | rs2020902 |
23andMe | rs2020902 |
SNPshot | rs2020902 |
SNPdbe | rs2020902 |
MSV3d | rs2020902 |
GWAS Ctlg | rs2020902 |
GMAF | 0.09826 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20855536] Germline Variation in Apoptosis Pathway Genes and Risk of non-Hodgkin Lymphoma