rs137852725

Orientation

plus

Stabilized

plus

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

Make rs137852725(C;T)

Make rs137852725(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137814479

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852725
dbSNP (classic)	rs137852725
ClinGen	rs137852725
ebi	rs137852725
HLI	rs137852725
Exac	rs137852725
Gnomad	rs137852725
Varsome	rs137852725
LitVar	rs137852725
Map	rs137852725
PheGenI	rs137852725
Biobank	rs137852725
1000 genomes	rs137852725
hgdp	rs137852725
ensembl	rs137852725
geneview	rs137852725
scholar	rs137852725
google	rs137852725
pharmgkb	rs137852725
gwascentral	rs137852725
openSNP	rs137852725
23andMe	rs137852725
SNPshot	rs137852725
SNPdbe	rs137852725
MSV3d	rs137852725
GWAS Ctlg	rs137852725

Max Magnitude

0

ClinVar
Risk	rs137852725(T;T)
Alt	rs137852725(T;T)
Reference	Rs137852725(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.140708931C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055966.1,