ClinVar Genomic variation as it relates to human health
GRCh38/hg38 9q34.3(chr9:137778047-137862670)x1
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
EHMT1 | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
1984 | 2216 | |
LOC108281115 | - | - | - | GRCh38 | - | 41 |
LOC130003149 | - | - | - | GRCh38 | - | 43 |
LOC130003150 | - | - | - | GRCh38 | - | 44 |
LOC651337 | - | - | - |
GRCh38 GRCh37 |
- | 121 |
MIR602 | - | - | - | GRCh38 | - | 41 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000051124.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024