rs137852721

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GT;GT)	0	common in clinvar
(TG;TG)	0	common in clinvar

Make rs137852721(-;-)

Make rs137852721(-;GT)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137811611

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852721
dbSNP (classic)	rs137852721
ClinGen	rs137852721
ebi	rs137852721
HLI	rs137852721
Exac	rs137852721
Gnomad	rs137852721
Varsome	rs137852721
LitVar	rs137852721
Map	rs137852721
PheGenI	rs137852721
Biobank	rs137852721
1000 genomes	rs137852721
hgdp	rs137852721
ensembl	rs137852721
geneview	rs137852721
scholar	rs137852721
google	rs137852721
pharmgkb	rs137852721
gwascentral	rs137852721
openSNP	rs137852721
23andMe	rs137852721
SNPshot	rs137852721
SNPdbe	rs137852721
MSV3d	rs137852721
GWAS Ctlg	rs137852721

Max Magnitude

0

ClinVar
Risk	rs137852721(-;-)
Alt	rs137852721(-;-)
Reference	Rs137852721(TG;TG)
Significance	Pathogenic
Disease	Chromosome 9q deletion syndrome
Variation	info
Gene	LOC101928853 EHMT1
CLNDBN	Chromosome 9q deletion syndrome
Reversed	0
HGVS	NC_000009.11:g.140706063_140706064delGT
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055962.1,