ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q24.3(chr16:89688616-89828326)x1
Germline
Classification
(1)
Uncertain significance
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 |
83 | 163 | |
CHMP1A | - | - |
GRCh38 GRCh37 |
198 | 276 | |
DPEP1 | - | - |
GRCh38 GRCh37 |
19 | 94 | |
FANCA | - | - |
GRCh38 GRCh37 |
4152 | 5300 | |
SPATA2L | - | - | - |
GRCh38 GRCh37 |
33 | 104 |
SPATA33 | - | - |
GRCh38 GRCh37 |
16 | 95 | |
VPS9D1 | - | - |
GRCh38 GRCh37 |
30 | 115 | |
ZNF276 | - | - |
GRCh38 GRCh37 |
46 | 863 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 29, 2017 | RCV000847869.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022