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rs137852727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852727(C;T)
Make rs137852727(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137834397
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852727
ebirs137852727
HLIrs137852727
Exacrs137852727
Varsomers137852727
Maprs137852727
PheGenIrs137852727
hapmaprs137852727
1000 genomesrs137852727
hgdprs137852727
ensemblrs137852727
gopubmedrs137852727
geneviewrs137852727
scholarrs137852727
googlers137852727
pharmgkbrs137852727
gwascentralrs137852727
openSNPrs137852727
23andMers137852727
23andMe allrs137852727
SNP Nexus

SNPshotrs137852727
SNPdbers137852727
MSV3drs137852727
GWAS Ctlgrs137852727
Max Magnitude0
ClinVar
Risk rs137852727(T;T)
Alt rs137852727(T;T)
Reference rs137852727(C;C)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140728849C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055967.1,