rs11152377
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11152377(C;C) |
Make rs11152377(C;T) |
Make rs11152377(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 18 |
Position | 63305213 |
Gene | BCL2 |
is a | snp |
is | mentioned by |
dbSNP | rs11152377 |
dbSNP (classic) | rs11152377 |
ClinGen | rs11152377 |
ebi | rs11152377 |
HLI | rs11152377 |
Exac | rs11152377 |
Gnomad | rs11152377 |
Varsome | rs11152377 |
LitVar | rs11152377 |
Map | rs11152377 |
PheGenI | rs11152377 |
Biobank | rs11152377 |
1000 genomes | rs11152377 |
hgdp | rs11152377 |
ensembl | rs11152377 |
geneview | rs11152377 |
scholar | rs11152377 |
rs11152377 | |
pharmgkb | rs11152377 |
gwascentral | rs11152377 |
openSNP | rs11152377 |
23andMe | rs11152377 |
SNPshot | rs11152377 |
SNPdbe | rs11152377 |
MSV3d | rs11152377 |
GWAS Ctlg | rs11152377 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27462919] Genetic variations in apoptosis pathway and the risk of ovarian cancer.