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rs137852724

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852724(G;T)
Make rs137852724(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137813531
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852724
ebirs137852724
HLIrs137852724
Exacrs137852724
Varsomers137852724
Maprs137852724
PheGenIrs137852724
hapmaprs137852724
1000 genomesrs137852724
hgdprs137852724
ensemblrs137852724
gopubmedrs137852724
geneviewrs137852724
scholarrs137852724
googlers137852724
pharmgkbrs137852724
gwascentralrs137852724
openSNPrs137852724
23andMers137852724
23andMe allrs137852724
SNP Nexus

SNPshotrs137852724
SNPdbers137852724
MSV3drs137852724
GWAS Ctlgrs137852724
Max Magnitude0
ClinVar
Risk rs137852724(T;T)
Alt rs137852724(T;T)
Reference rs137852724(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.140707983G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055965.1,