ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3
Germline
Classification
(1)
Pathogenic
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 | |||
RET | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3446 | 3566 | |
CTNNA3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
933 | 998 | |
EGR2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
397 | 421 | |
GDF2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
246 | 361 | |
A1CF | - | - |
GRCh38 GRCh37 |
22 | 42 | |
ADO | - | - |
GRCh38 GRCh37 |
5 | 25 | |
AGAP10 | - | - | - | GRCh37 | - | 100 |
AGAP4 | - | - | - |
GRCh38 GRCh37 |
52 | 87 |
AGAP6 | - | - | - |
GRCh38 GRCh37 |
- | 107 |
AGAP9 | - | - | - |
GRCh38 GRCh37 |
- | 107 |
There are 553 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 20, 2012 | RCV000142967.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023