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rs41277434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41277434(A;C)
Make rs41277434(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position148809304
GeneEZH2
is asnp
is mentioned by
dbSNPrs41277434
ebirs41277434
HLIrs41277434
Exacrs41277434
Varsomers41277434
Maprs41277434
PheGenIrs41277434
hapmaprs41277434
1000 genomesrs41277434
hgdprs41277434
ensemblrs41277434
gopubmedrs41277434
geneviewrs41277434
scholarrs41277434
googlers41277434
pharmgkbrs41277434
gwascentralrs41277434
openSNPrs41277434
23andMers41277434
23andMe allrs41277434
SNP Nexus

SNPshotrs41277434
SNPdbers41277434
MSV3drs41277434
GWAS Ctlgrs41277434
Max Magnitude0

[PMID 24040354OA-icon.png] Effects of EZH2 polymorphisms on susceptibility to and pathological development of hepatocellular carcinoma


ClinVar
Risk rs41277434(C,G;C,G)
Alt rs41277434(C,G;C,G)
Reference rs41277434(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene EZH2
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.148506396A>C; NC_000007.13:g.148506396A>G
CLNSRC ClinVar GeneDx University of Chicago
CLNACC RCV000145977.3, RCV000145976.1,



[PMID 24691023OA-icon.png] Impact of EZH2 polymorphisms on urothelial cell carcinoma susceptibility and clinicopathologic features