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rs121918301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918301(C;T)
Make rs121918301(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137818100
GeneEHMT1
is asnp
is mentioned by
dbSNPrs121918301
ebirs121918301
HLIrs121918301
Exacrs121918301
Varsomers121918301
Maprs121918301
PheGenIrs121918301
hapmaprs121918301
1000 genomesrs121918301
hgdprs121918301
ensemblrs121918301
gopubmedrs121918301
geneviewrs121918301
scholarrs121918301
googlers121918301
pharmgkbrs121918301
gwascentralrs121918301
openSNPrs121918301
23andMers121918301
23andMe allrs121918301
SNP Nexus

SNPshotrs121918301
SNPdbers121918301
MSV3drs121918301
GWAS Ctlgrs121918301
Max Magnitude0
OMIM607001
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918301(T;T)
Alt rs121918301(T;T)
Reference rs121918301(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.140712552C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003789.2,