ClinVar Genomic variation as it relates to human health
NM_170675.5(MEIS2):c.460C>A (p.Leu154Ile)
Germline
Classification
(2)
Uncertain significance
criteria provided, multiple submitters, no conflicts
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 | |||
MEIS2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
136 | 158 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 27, 2022 | RCV002882584.1 | |
Uncertain significance (1) |
|
Feb 26, 2023 | RCV003324868.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 03, 2023