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rs137852720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852720(C;C)
Make rs137852720(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137779634
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852720
ebirs137852720
HLIrs137852720
Exacrs137852720
Varsomers137852720
Maprs137852720
PheGenIrs137852720
hapmaprs137852720
1000 genomesrs137852720
hgdprs137852720
ensemblrs137852720
gopubmedrs137852720
geneviewrs137852720
scholarrs137852720
googlers137852720
pharmgkbrs137852720
gwascentralrs137852720
openSNPrs137852720
23andMers137852720
23andMe allrs137852720
SNP Nexus

SNPshotrs137852720
SNPdbers137852720
MSV3drs137852720
GWAS Ctlgrs137852720
Max Magnitude0
ClinVar
Risk rs137852720(C;C)
Alt rs137852720(C;C)
Reference rs137852720(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.140674086G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055961.1,