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rs137852719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs137852719(-;-)
Make rs137852719(-;G)
Make rs137852719(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137777892
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852719
ebirs137852719
HLIrs137852719
Exacrs137852719
Varsomers137852719
Maprs137852719
PheGenIrs137852719
hapmaprs137852719
1000 genomesrs137852719
hgdprs137852719
ensemblrs137852719
gopubmedrs137852719
geneviewrs137852719
scholarrs137852719
googlers137852719
pharmgkbrs137852719
gwascentralrs137852719
openSNPrs137852719
23andMers137852719
23andMe allrs137852719
SNP Nexus

SNPshotrs137852719
SNPdbers137852719
MSV3drs137852719
GWAS Ctlgrs137852719
Max Magnitude0
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