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rs1057519894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519894(A;T)
Make rs1057519894(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position148811650
GeneEZH2
is asnp
is mentioned by
dbSNPrs1057519894
dbSNP (classic)rs1057519894
ClinGenrs1057519894
ebirs1057519894
HLIrs1057519894
Exacrs1057519894
Gnomadrs1057519894
Varsomers1057519894
LitVarrs1057519894
Maprs1057519894
PheGenIrs1057519894
Biobankrs1057519894
1000 genomesrs1057519894
hgdprs1057519894
ensemblrs1057519894
geneviewrs1057519894
scholarrs1057519894
googlers1057519894
pharmgkbrs1057519894
gwascentralrs1057519894
openSNPrs1057519894
23andMers1057519894
23andMe allrs1057519894
SNPshotrs1057519894
SNPdbers1057519894
MSV3drs1057519894
GWAS Ctlgrs1057519894
Max Magnitude0
ClinVar
Risk rs1057519894(C;C) rs1057519894(T;T)
Alt rs1057519894(C;C) rs1057519894(T;T)
Reference Rs1057519894(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Malignant lymphoma
Variation info
Gene EZH2
CLNDBN Malignant melanoma of skin Malignant lymphoma, non-Hodgkin
Reversed 1
HGVS NC_000007.13:g.148508742T>A; NC_000007.13:g.148508742T>G
CLNSRC
CLNACC RCV000419957.1, RCV000437178.1, RCV000429761.1, RCV000436936.1,