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rs137852721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs137852721(-;-)
Make rs137852721(-;GT)
ReferenceGRCh38 38.1/141
Chromosome9
Position137811611
GeneEHMT1
is asnp
is mentioned by
dbSNPrs137852721
ebirs137852721
HLIrs137852721
Exacrs137852721
Varsomers137852721
Maprs137852721
PheGenIrs137852721
hapmaprs137852721
1000 genomesrs137852721
hgdprs137852721
ensemblrs137852721
gopubmedrs137852721
geneviewrs137852721
scholarrs137852721
googlers137852721
pharmgkbrs137852721
gwascentralrs137852721
openSNPrs137852721
23andMers137852721
23andMe allrs137852721
SNP Nexus

SNPshotrs137852721
SNPdbers137852721
MSV3drs137852721
GWAS Ctlgrs137852721
Max Magnitude0
ClinVar
Risk rs137852721(;)
Alt rs137852721(;)
Reference rs137852721(TG;TG)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene LOC101928853 EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140706063_140706064delGT
CLNSRC ClinVar GeneReviews
CLNACC RCV000055962.1,