rs11708581
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11708581(A;A) |
Make rs11708581(A;C) |
Make rs11708581(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 52394972 |
Gene | DNAH1 |
is a | snp |
is | mentioned by |
dbSNP | rs11708581 |
dbSNP (classic) | rs11708581 |
ClinGen | rs11708581 |
ebi | rs11708581 |
HLI | rs11708581 |
Exac | rs11708581 |
Gnomad | rs11708581 |
Varsome | rs11708581 |
LitVar | rs11708581 |
Map | rs11708581 |
PheGenI | rs11708581 |
Biobank | rs11708581 |
1000 genomes | rs11708581 |
hgdp | rs11708581 |
ensembl | rs11708581 |
geneview | rs11708581 |
scholar | rs11708581 |
rs11708581 | |
pharmgkb | rs11708581 |
gwascentral | rs11708581 |
openSNP | rs11708581 |
23andMe | rs11708581 |
SNPshot | rs11708581 |
SNPdbe | rs11708581 |
MSV3d | rs11708581 |
GWAS Ctlg | rs11708581 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 29088836] Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.