rs137852724

Orientation

plus

Stabilized

plus

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

Make rs137852724(G;T)

Make rs137852724(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137813531

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852724
dbSNP (classic)	rs137852724
ClinGen	rs137852724
ebi	rs137852724
HLI	rs137852724
Exac	rs137852724
Gnomad	rs137852724
Varsome	rs137852724
LitVar	rs137852724
Map	rs137852724
PheGenI	rs137852724
Biobank	rs137852724
1000 genomes	rs137852724
hgdp	rs137852724
ensembl	rs137852724
geneview	rs137852724
scholar	rs137852724
google	rs137852724
pharmgkb	rs137852724
gwascentral	rs137852724
openSNP	rs137852724
23andMe	rs137852724
SNPshot	rs137852724
SNPdbe	rs137852724
MSV3d	rs137852724
GWAS Ctlg	rs137852724

Max Magnitude

0

ClinVar
Risk	rs137852724(T;T)
Alt	rs137852724(T;T)
Reference	Rs137852724(G;G)
Significance	Pathogenic
Disease	Chromosome 9q deletion syndrome
Variation	info
Gene	EHMT1
CLNDBN	Chromosome 9q deletion syndrome
Reversed	0
HGVS	NC_000009.11:g.140707983G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055965.1,