Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs267601394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267601394(A;A)
Make rs267601394(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position148811635
GeneEZH2
is asnp
is mentioned by
dbSNPrs267601394
dbSNP (old)rs267601394
ClinGenrs267601394
ebirs267601394
HLIrs267601394
Exacrs267601394
Gnomadrs267601394
Varsomers267601394
Maprs267601394
PheGenIrs267601394
Biobankrs267601394
1000 genomesrs267601394
hgdprs267601394
ensemblrs267601394
gopubmedrs267601394
geneviewrs267601394
scholarrs267601394
googlers267601394
pharmgkbrs267601394
gwascentralrs267601394
openSNPrs267601394
23andMers267601394
23andMe allrs267601394
SNPshotrs267601394
SNPdbers267601394
MSV3drs267601394
GWAS Ctlgrs267601394
Max Magnitude0
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,