rs137852726

Orientation

plus

Stabilized

plus

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

Make rs137852726(A;A)

Make rs137852726(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137814468

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852726
dbSNP (classic)	rs137852726
ClinGen	rs137852726
ebi	rs137852726
HLI	rs137852726
Exac	rs137852726
Gnomad	rs137852726
Varsome	rs137852726
LitVar	rs137852726
Map	rs137852726
PheGenI	rs137852726
Biobank	rs137852726
1000 genomes	rs137852726
hgdp	rs137852726
ensembl	rs137852726
geneview	rs137852726
scholar	rs137852726
google	rs137852726
pharmgkb	rs137852726
gwascentral	rs137852726
openSNP	rs137852726
23andMe	rs137852726
SNPshot	rs137852726
SNPdbe	rs137852726
MSV3d	rs137852726
GWAS Ctlg	rs137852726

Max Magnitude

0

OMIM	607001
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137852726(A;A)
Alt	rs137852726(A;A)
Reference	Rs137852726(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.140708920G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003791.2,