rs886039601

Orientation

minus

Stabilized

minus

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

Make rs886039601(C;G)

Make rs886039601(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

148810355

Gene

EZH2

is a	snp
is	mentioned by
dbSNP	rs886039601
dbSNP (classic)	rs886039601
ClinGen	rs886039601
ebi	rs886039601
HLI	rs886039601
Exac	rs886039601
Gnomad	rs886039601
Varsome	rs886039601
LitVar	rs886039601
Map	rs886039601
PheGenI	rs886039601
Biobank	rs886039601
1000 genomes	rs886039601
hgdp	rs886039601
ensembl	rs886039601
geneview	rs886039601
scholar	rs886039601
google	rs886039601
pharmgkb	rs886039601
gwascentral	rs886039601
openSNP	rs886039601
23andMe	rs886039601
SNPshot	rs886039601
SNPdbe	rs886039601
MSV3d	rs886039601
GWAS Ctlg	rs886039601

Max Magnitude

0

ClinVar
Risk	rs886039601(G;G)
Alt	rs886039601(G;G)
Reference	Rs886039601(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	EZH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.148507447G>C
CLNSRC
CLNACC	RCV000256045.1,