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rs137852725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852725(C;T)
Make rs137852725(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137814479
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852725
ClinGenrs137852725
ebirs137852725
HLIrs137852725
Exacrs137852725
Varsomers137852725
Maprs137852725
PheGenIrs137852725
Biobankrs137852725
1000 genomesrs137852725
hgdprs137852725
ensemblrs137852725
gopubmedrs137852725
geneviewrs137852725
scholarrs137852725
googlers137852725
pharmgkbrs137852725
gwascentralrs137852725
openSNPrs137852725
23andMers137852725
23andMe allrs137852725
SNP Nexus

SNPshotrs137852725
SNPdbers137852725
MSV3drs137852725
GWAS Ctlgrs137852725
Max Magnitude0
ClinVar
Risk rs137852725(T;T)
Alt rs137852725(T;T)
Reference Rs137852725(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.140708931C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055966.1,