rs137852722

Orientation

plus

Stabilized

plus

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

Make rs137852722(A;A)

Make rs137852722(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137813005

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852722
dbSNP (classic)	rs137852722
ClinGen	rs137852722
ebi	rs137852722
HLI	rs137852722
Exac	rs137852722
Gnomad	rs137852722
Varsome	rs137852722
LitVar	rs137852722
Map	rs137852722
PheGenI	rs137852722
Biobank	rs137852722
1000 genomes	rs137852722
hgdp	rs137852722
ensembl	rs137852722
geneview	rs137852722
scholar	rs137852722
google	rs137852722
pharmgkb	rs137852722
gwascentral	rs137852722
openSNP	rs137852722
23andMe	rs137852722
SNPshot	rs137852722
SNPdbe	rs137852722
MSV3d	rs137852722
GWAS Ctlg	rs137852722

Max Magnitude

0

ClinVar
Risk	rs137852722(A;A)
Alt	rs137852722(A;A)
Reference	Rs137852722(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.140707457G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055963.1,