rs267601394
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs267601394(A;A) |
Make rs267601394(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 148811635 |
Gene | EZH2 |
is a | snp |
is | mentioned by |
dbSNP | rs267601394 |
dbSNP (classic) | rs267601394 |
ClinGen | rs267601394 |
ebi | rs267601394 |
HLI | rs267601394 |
Exac | rs267601394 |
Gnomad | rs267601394 |
Varsome | rs267601394 |
LitVar | rs267601394 |
Map | rs267601394 |
PheGenI | rs267601394 |
Biobank | rs267601394 |
1000 genomes | rs267601394 |
hgdp | rs267601394 |
ensembl | rs267601394 |
geneview | rs267601394 |
scholar | rs267601394 |
rs267601394 | |
pharmgkb | rs267601394 |
gwascentral | rs267601394 |
openSNP | rs267601394 |
23andMe | rs267601394 |
SNPshot | rs267601394 |
SNPdbe | rs267601394 |
MSV3d | rs267601394 |
GWAS Ctlg | rs267601394 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs267601394(A;A) rs267601394(G;G) |
Alt | rs267601394(A;A) rs267601394(G;G) |
Reference | Rs267601394(T;T) |
Significance | Probable-Pathogenic |
Disease | Malignant lymphoma Lymphoma Malignant melanoma of skin |
Variation | info |
Gene | EZH2 |
CLNDBN | Malignant lymphoma, non-Hodgkin Lymphoma Malignant melanoma of skin |
Reversed | 0 |
HGVS | NC_000007.13:g.148508727T>A; NC_000007.13:g.148508727T>G |
CLNSRC | |
CLNACC | RCV000422926.1, RCV000430342.1, RCV000440575.1, RCV000423969.1, RCV000433156.1, RCV000441670.1, |