rs137852720

Orientation

plus

Stabilized

plus

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

Make rs137852720(C;C)

Make rs137852720(C;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137779634

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852720
dbSNP (classic)	rs137852720
ClinGen	rs137852720
ebi	rs137852720
HLI	rs137852720
Exac	rs137852720
Gnomad	rs137852720
Varsome	rs137852720
LitVar	rs137852720
Map	rs137852720
PheGenI	rs137852720
Biobank	rs137852720
1000 genomes	rs137852720
hgdp	rs137852720
ensembl	rs137852720
geneview	rs137852720
scholar	rs137852720
google	rs137852720
pharmgkb	rs137852720
gwascentral	rs137852720
openSNP	rs137852720
23andMe	rs137852720
SNPshot	rs137852720
SNPdbe	rs137852720
MSV3d	rs137852720
GWAS Ctlg	rs137852720

Max Magnitude

0

ClinVar
Risk	rs137852720(C;C)
Alt	rs137852720(C;C)
Reference	Rs137852720(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.140674086G>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055961.1,