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rs267601395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267601395(A;G)
Make rs267601395(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position148811636
GeneEZH2
is asnp
is mentioned by
dbSNPrs267601395
dbSNP (old)rs267601395
ClinGenrs267601395
ebirs267601395
HLIrs267601395
Exacrs267601395
Gnomadrs267601395
Varsomers267601395
Maprs267601395
PheGenIrs267601395
Biobankrs267601395
1000 genomesrs267601395
hgdprs267601395
ensemblrs267601395
gopubmedrs267601395
geneviewrs267601395
scholarrs267601395
googlers267601395
pharmgkbrs267601395
gwascentralrs267601395
openSNPrs267601395
23andMers267601395
23andMe allrs267601395
SNPshotrs267601395
SNPdbers267601395
MSV3drs267601395
GWAS Ctlgrs267601395
Max Magnitude0
ClinVar
Risk rs267601395(G;G) rs267601395(T;T)
Alt rs267601395(G;G) rs267601395(T;T)
Reference Rs267601395(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Lymphoma Malignant lymphoma
Variation info
Gene EZH2
CLNDBN Malignant melanoma of skin Lymphoma Malignant lymphoma, non-Hodgkin
Reversed 0
HGVS NC_000007.13:g.148508728A>G; NC_000007.13:g.148508728A>T
CLNSRC
CLNACC RCV000418998.1, RCV000429291.1, RCV000436489.1, RCV000421839.1, RCV000429270.1, RCV000439496.1,