rs137852727

Orientation

plus

Stabilized

plus

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

Make rs137852727(C;T)

Make rs137852727(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137834397

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852727
dbSNP (classic)	rs137852727
ClinGen	rs137852727
ebi	rs137852727
HLI	rs137852727
Exac	rs137852727
Gnomad	rs137852727
Varsome	rs137852727
LitVar	rs137852727
Map	rs137852727
PheGenI	rs137852727
Biobank	rs137852727
1000 genomes	rs137852727
hgdp	rs137852727
ensembl	rs137852727
geneview	rs137852727
scholar	rs137852727
google	rs137852727
pharmgkb	rs137852727
gwascentral	rs137852727
openSNP	rs137852727
23andMe	rs137852727
SNPshot	rs137852727
SNPdbe	rs137852727
MSV3d	rs137852727
GWAS Ctlg	rs137852727

Max Magnitude

0

ClinVar
Risk	rs137852727(T;T)
Alt	rs137852727(T;T)
Reference	Rs137852727(C;C)
Significance	Pathogenic
Disease	Chromosome 9q deletion syndrome
Variation	info
Gene	EHMT1
CLNDBN	Chromosome 9q deletion syndrome
Reversed	0
HGVS	NC_000009.11:g.140728849C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055967.1,