rs137852723

Orientation

plus

Stabilized

plus

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

Make rs137852723(-;-)

Make rs137852723(-;TCTC)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137813016

Gene

EHMT1

is a	snp
is	mentioned by
dbSNP	rs137852723
dbSNP (classic)	rs137852723
ClinGen	rs137852723
ebi	rs137852723
HLI	rs137852723
Exac	rs137852723
Gnomad	rs137852723
Varsome	rs137852723
LitVar	rs137852723
Map	rs137852723
PheGenI	rs137852723
Biobank	rs137852723
1000 genomes	rs137852723
hgdp	rs137852723
ensembl	rs137852723
geneview	rs137852723
scholar	rs137852723
google	rs137852723
pharmgkb	rs137852723
gwascentral	rs137852723
openSNP	rs137852723
23andMe	rs137852723
SNPshot	rs137852723
SNPdbe	rs137852723
MSV3d	rs137852723
GWAS Ctlg	rs137852723

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs137852723(TCTC;TCTC)
Significance	Pathogenic
Disease	Chromosome 9q deletion syndrome
Variation	info
Gene	EHMT1
CLNDBN	Chromosome 9q deletion syndrome
Reversed	0
HGVS	NC_000009.11:g.140707468_140707471delTCTC
CLNSRC
CLNACC