rs7585356
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7585356(A;A) |
Make rs7585356(A;G) |
Make rs7585356(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 214727582 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs7585356 |
dbSNP (classic) | rs7585356 |
ClinGen | rs7585356 |
ebi | rs7585356 |
HLI | rs7585356 |
Exac | rs7585356 |
Gnomad | rs7585356 |
Varsome | rs7585356 |
LitVar | rs7585356 |
Map | rs7585356 |
PheGenI | rs7585356 |
Biobank | rs7585356 |
1000 genomes | rs7585356 |
hgdp | rs7585356 |
ensembl | rs7585356 |
geneview | rs7585356 |
scholar | rs7585356 |
rs7585356 | |
pharmgkb | rs7585356 |
gwascentral | rs7585356 |
openSNP | rs7585356 |
23andMe | rs7585356 |
SNPshot | rs7585356 |
SNPdbe | rs7585356 |
MSV3d | rs7585356 |
GWAS Ctlg | rs7585356 |
GMAF | 0.2759 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23222812] Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility
[PMID 19412175] Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.