ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p14.1(chr11:27340839-27572771)x1
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 | |||
BDNF-AS | - | - |
GRCh38 GRCh37 |
- | 135 | |
CCDC34 | - | - |
GRCh38 GRCh37 |
14 | 34 | |
LGR4 | - | - |
GRCh38 GRCh37 |
70 | 100 | |
LIN7C | - | - |
GRCh38 GRCh37 |
4 | 27 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 17, 2021 | RCV002474961.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022