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rs137852722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852722(A;A)
Make rs137852722(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137813005
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852722
ebirs137852722
HLIrs137852722
Exacrs137852722
Varsomers137852722
Maprs137852722
PheGenIrs137852722
hapmaprs137852722
1000 genomesrs137852722
hgdprs137852722
ensemblrs137852722
gopubmedrs137852722
geneviewrs137852722
scholarrs137852722
googlers137852722
pharmgkbrs137852722
gwascentralrs137852722
openSNPrs137852722
23andMers137852722
23andMe allrs137852722
SNP Nexus

SNPshotrs137852722
SNPdbers137852722
MSV3drs137852722
GWAS Ctlgrs137852722
Max Magnitude0
ClinVar
Risk rs137852722(A;A)
Alt rs137852722(A;A)
Reference rs137852722(G;G)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140707457G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000055963.1,