ClinVar Genomic variation as it relates to human health
NM_001387274.1(DCDC1):c.754+9G>T
Germline
Classification
(2)
Likely benign
criteria provided, multiple submitters, no conflicts
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 |
58 | 123 | |
LOC126861175 | - | - | - | GRCh38 | - | 26 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Sep 3, 2022 | RCV002900056.2 | |
Likely benign (1) |
|
Jul 11, 2019 | RCV003961155.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 17, 2024