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rs137852726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852726(A;A)
Make rs137852726(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137814468
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852726
ebirs137852726
HLIrs137852726
Exacrs137852726
Varsomers137852726
Maprs137852726
PheGenIrs137852726
hapmaprs137852726
1000 genomesrs137852726
hgdprs137852726
ensemblrs137852726
gopubmedrs137852726
geneviewrs137852726
scholarrs137852726
googlers137852726
pharmgkbrs137852726
gwascentralrs137852726
openSNPrs137852726
23andMers137852726
23andMe allrs137852726
SNP Nexus

SNPshotrs137852726
SNPdbers137852726
MSV3drs137852726
GWAS Ctlgrs137852726
Max Magnitude0
OMIM607001
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852726(A;A)
Alt rs137852726(A;A)
Reference rs137852726(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.140708920G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003791.2,