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rs137852723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCTC;TCTC) 0 common in clinvar
Make rs137852723(-;-)
Make rs137852723(-;TCTC)
ReferenceGRCh38 38.1/141
Chromosome9
Position137813016
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852723
ebirs137852723
HLIrs137852723
Exacrs137852723
Varsomers137852723
Maprs137852723
PheGenIrs137852723
hapmaprs137852723
1000 genomesrs137852723
hgdprs137852723
ensemblrs137852723
gopubmedrs137852723
geneviewrs137852723
scholarrs137852723
googlers137852723
pharmgkbrs137852723
gwascentralrs137852723
openSNPrs137852723
23andMers137852723
23andMe allrs137852723
SNP Nexus

SNPshotrs137852723
SNPdbers137852723
MSV3drs137852723
GWAS Ctlgrs137852723
Max Magnitude0
ClinVar
Risk rs137852723(;)
Alt rs137852723(;)
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