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rs1057519833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519833(C;G)
Make rs1057519833(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position148809375
GeneEZH2
is asnp
is mentioned by
dbSNPrs1057519833
dbSNP (classic)rs1057519833
ClinGenrs1057519833
ebirs1057519833
HLIrs1057519833
Exacrs1057519833
Gnomadrs1057519833
Varsomers1057519833
LitVarrs1057519833
Maprs1057519833
PheGenIrs1057519833
Biobankrs1057519833
1000 genomesrs1057519833
hgdprs1057519833
ensemblrs1057519833
geneviewrs1057519833
scholarrs1057519833
googlers1057519833
pharmgkbrs1057519833
gwascentralrs1057519833
openSNPrs1057519833
23andMers1057519833
SNPshotrs1057519833
SNPdbers1057519833
MSV3drs1057519833
GWAS Ctlgrs1057519833
Max Magnitude0
ClinVar
Risk rs1057519833(G;G)
Alt rs1057519833(G;G)
Reference Rs1057519833(C;C)
Significance Probable-Pathogenic
Disease Lymphoma
Variation info
Gene EZH2
CLNDBN Lymphoma
Reversed 1
HGVS NC_000007.13:g.148506467G>C
CLNSRC
CLNACC RCV000434252.1,