rs41277434

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs41277434(A;C)

Make rs41277434(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

148809304

Gene

EZH2

is a	snp
is	mentioned by
dbSNP	rs41277434
dbSNP (classic)	rs41277434
ClinGen	rs41277434
ebi	rs41277434
HLI	rs41277434
Exac	rs41277434
Gnomad	rs41277434
Varsome	rs41277434
LitVar	rs41277434
Map	rs41277434
PheGenI	rs41277434
Biobank	rs41277434
1000 genomes	rs41277434
hgdp	rs41277434
ensembl	rs41277434
geneview	rs41277434
scholar	rs41277434
google	rs41277434
pharmgkb	rs41277434
gwascentral	rs41277434
openSNP	rs41277434
23andMe	rs41277434
SNPshot	rs41277434
SNPdbe	rs41277434
MSV3d	rs41277434
GWAS Ctlg	rs41277434

Max Magnitude

0

[PMID 24040354] Effects of EZH2 polymorphisms on susceptibility to and pathological development of hepatocellular carcinoma

ClinVar
Risk	rs41277434(C;C) rs41277434(G;G)
Alt	rs41277434(C;C) rs41277434(G;G)
Reference	Rs41277434(A;A)
Significance	Non-pathogenic
Disease	not specified Weaver syndrome
Variation	info
Gene	EZH2
CLNDBN	not specified Weaver syndrome
Reversed	0
HGVS	NC_000007.13:g.148506396A>C; NC_000007.13:g.148506396A>G
CLNSRC	ClinVar GeneDx University of Chicago
CLNACC	RCV000145977.4, RCV000358908.1, RCV000145976.1,

[PMID 24691023] Impact of EZH2 polymorphisms on urothelial cell carcinoma susceptibility and clinicopathologic features