ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q24.3(chr16:89748800-89903843)x1
Germline
Classification
(1)
Likely benign
no assertion criteria provided
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 | |||
CDK10 | - | - |
GRCh38 GRCh37 |
85 | 166 | |
FANCA | - | - |
GRCh38 GRCh37 |
4165 | 5320 | |
SPATA2L | - | - | - |
GRCh38 GRCh37 |
37 | 108 |
SPIRE2 | - | - |
GRCh38 GRCh37 |
82 | 160 | |
VPS9D1 | - | - |
GRCh38 GRCh37 |
32 | 120 | |
ZNF276 | - | - |
GRCh38 GRCh37 |
52 | 875 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 15, 2020 | RCV001827933.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 17, 2022