ClinVar Genomic variation as it relates to human health
NM_014921.5(ADGRL1):c.3325C>T (p.His1109Tyr)
Germline
Classification
(1)
Uncertain significance
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 | |||
ADGRL1 | - | - |
GRCh38 GRCh38 GRCh37 |
9 | 172 | |
ADGRL1-AS1 | - | - | - |
GRCh38 GRCh38 |
- | 154 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 1, 2024 | RCV004547171.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 04, 2024