ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q24.3(chr14:76740491-77334658)x3
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 | |||
ANGEL1 | - | - |
GRCh38 GRCh37 |
43 | 64 | |
ESRRB | - | - |
GRCh38 GRCh37 |
250 | 273 | |
LRRC74A | - | - | - |
GRCh38 GRCh37 |
37 | 58 |
VASH1 | - | - |
GRCh38 GRCh37 |
22 | 43 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003987054.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024