ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p13(chr11:31001762-31555701)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 | |||
DCDC1 | - | - |
GRCh38 GRCh37 |
70 | 137 | |
DNAJC24 | - | - |
GRCh38 GRCh37 |
5 | 63 | |
ELP4 | - | - |
GRCh38 GRCh37 |
62 | 288 | |
IMMP1L | - | - |
GRCh38 GRCh37 |
11 | 73 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986933.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024