rs6950683
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6950683(C;C) |
Make rs6950683(C;T) |
Make rs6950683(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 148884496 |
Gene | EZH2 |
is a | snp |
is | mentioned by |
dbSNP | rs6950683 |
dbSNP (classic) | rs6950683 |
ClinGen | rs6950683 |
ebi | rs6950683 |
HLI | rs6950683 |
Exac | rs6950683 |
Gnomad | rs6950683 |
Varsome | rs6950683 |
LitVar | rs6950683 |
Map | rs6950683 |
PheGenI | rs6950683 |
Biobank | rs6950683 |
1000 genomes | rs6950683 |
hgdp | rs6950683 |
ensembl | rs6950683 |
geneview | rs6950683 |
scholar | rs6950683 |
rs6950683 | |
pharmgkb | rs6950683 |
gwascentral | rs6950683 |
openSNP | rs6950683 |
23andMe | rs6950683 |
SNPshot | rs6950683 |
SNPdbe | rs6950683 |
MSV3d | rs6950683 |
GWAS Ctlg | rs6950683 |
Max Magnitude | 0 |
[PMID 24040354] Effects of EZH2 polymorphisms on susceptibility to and pathological development of hepatocellular carcinoma
[PMID 24691023] Impact of EZH2 polymorphisms on urothelial cell carcinoma susceptibility and clinicopathologic features
[PMID 32748461] EZH2 Polymorphisms in melanoma skin cancer risk.