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rs137852716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAC;AGAC) 0 common in clinvar
Make rs137852716(-;-)
Make rs137852716(-;AGAC)
ReferenceGRCh38 38.1/141
Chromosome9
Position137762706
GeneEHMT1, ZNF219
is asnp
is mentioned by
dbSNPrs137852716
ebirs137852716
HLIrs137852716
Exacrs137852716
Varsomers137852716
Maprs137852716
PheGenIrs137852716
hapmaprs137852716
1000 genomesrs137852716
hgdprs137852716
ensemblrs137852716
gopubmedrs137852716
geneviewrs137852716
scholarrs137852716
googlers137852716
pharmgkbrs137852716
gwascentralrs137852716
openSNPrs137852716
23andMers137852716
23andMe allrs137852716
SNP Nexus

SNPshotrs137852716
SNPdbers137852716
MSV3drs137852716
GWAS Ctlgrs137852716
Max Magnitude0
ClinVar
Risk rs137852716(;)
Alt rs137852716(;)
Reference rs137852716(AGAC;AGAC)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1-IT1 EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140657158_140657161delAGAC
CLNSRC ClinVar GeneReviews
CLNACC RCV000055956.1,