rs267601395

Orientation

plus

Stabilized

plus

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

Make rs267601395(A;G)

Make rs267601395(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

148811636

Gene

EZH2

is a	snp
is	mentioned by
dbSNP	rs267601395
dbSNP (classic)	rs267601395
ClinGen	rs267601395
ebi	rs267601395
HLI	rs267601395
Exac	rs267601395
Gnomad	rs267601395
Varsome	rs267601395
LitVar	rs267601395
Map	rs267601395
PheGenI	rs267601395
Biobank	rs267601395
1000 genomes	rs267601395
hgdp	rs267601395
ensembl	rs267601395
geneview	rs267601395
scholar	rs267601395
google	rs267601395
pharmgkb	rs267601395
gwascentral	rs267601395
openSNP	rs267601395
23andMe	rs267601395
SNPshot	rs267601395
SNPdbe	rs267601395
MSV3d	rs267601395
GWAS Ctlg	rs267601395

Max Magnitude

0

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,