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rs879255531

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255531(C;T)
Make rs879255531(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position137728379
GeneEHMT1
is asnp
is mentioned by
dbSNPrs879255531
ebirs879255531
HLIrs879255531
Exacrs879255531
Varsomers879255531
Maprs879255531
PheGenIrs879255531
hapmaprs879255531
1000 genomesrs879255531
hgdprs879255531
ensemblrs879255531
gopubmedrs879255531
geneviewrs879255531
scholarrs879255531
googlers879255531
pharmgkbrs879255531
gwascentralrs879255531
openSNPrs879255531
23andMers879255531
23andMe allrs879255531
SNP Nexus

SNPshotrs879255531
SNPdbers879255531
MSV3drs879255531
GWAS Ctlgrs879255531
Max Magnitude0
ClinVar
Risk rs879255531(T;T)
Alt rs879255531(T;T)
Reference rs879255531(C;C)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140622831C>T
CLNSRC
CLNACC RCV000239430.1,