rs12163565
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12163565(A;A) |
Make rs12163565(A;G) |
Make rs12163565(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 52396510 |
Gene | DNAH1 |
is a | snp |
is | mentioned by |
dbSNP | rs12163565 |
dbSNP (classic) | rs12163565 |
ClinGen | rs12163565 |
ebi | rs12163565 |
HLI | rs12163565 |
Exac | rs12163565 |
Gnomad | rs12163565 |
Varsome | rs12163565 |
LitVar | rs12163565 |
Map | rs12163565 |
PheGenI | rs12163565 |
Biobank | rs12163565 |
1000 genomes | rs12163565 |
hgdp | rs12163565 |
ensembl | rs12163565 |
geneview | rs12163565 |
scholar | rs12163565 |
rs12163565 | |
pharmgkb | rs12163565 |
gwascentral | rs12163565 |
openSNP | rs12163565 |
23andMe | rs12163565 |
SNPshot | rs12163565 |
SNPdbe | rs12163565 |
MSV3d | rs12163565 |
GWAS Ctlg | rs12163565 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29088836] Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.