ClinVar Genomic variation as it relates to human health
NM_145309.6(LRRC51):c.468C>T (p.Ile156=)
Germline
Classification
(1)
Likely benign
no assertion criteria provided
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 | |||
LRRC51 | - | - | - | GRCh38 | - | 48 |
LRTOMT | - | - |
GRCh38 GRCh37 |
23 | 239 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
LRTOMT-related disorder
|
Likely benign (1) |
|
Jul 30, 2019 | RCV003906894.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024