ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10p13(chr10:12961671-13207227)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 | |||
CCDC3 | - | - | - |
GRCh38 GRCh37 |
26 | 58 |
MCM10 | - | - |
GRCh38 GRCh37 |
80 | 108 | |
OPTN | - | - |
GRCh38 GRCh37 |
367 | 498 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 3, 2018 | RCV000847743.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022