rs137852719

Orientation

plus

Stabilized

plus

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

Make rs137852719(-;G)

Make rs137852719(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137777892

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852719
dbSNP (classic)	rs137852719
ClinGen	rs137852719
ebi	rs137852719
HLI	rs137852719
Exac	rs137852719
Gnomad	rs137852719
Varsome	rs137852719
LitVar	rs137852719
Map	rs137852719
PheGenI	rs137852719
Biobank	rs137852719
1000 genomes	rs137852719
hgdp	rs137852719
ensembl	rs137852719
geneview	rs137852719
scholar	rs137852719
google	rs137852719
pharmgkb	rs137852719
gwascentral	rs137852719
openSNP	rs137852719
23andMe	rs137852719
SNPshot	rs137852719
SNPdbe	rs137852719
MSV3d	rs137852719
GWAS Ctlg	rs137852719

Max Magnitude

0

ClinVar
Risk	rs137852719(G;G)
Alt	rs137852719(G;G)
Reference	Rs137852719(;)
Significance	Pathogenic
Disease	Chromosome 9q deletion syndrome
Variation	info
Gene	EHMT1
CLNDBN	Chromosome 9q deletion syndrome
Reversed	0
HGVS	NC_000009.11:g.140672344_140672345insG
CLNSRC
CLNACC