ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3p13-11.1(chr3:73824871-90453699)x1
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 | |||
ROBO1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
470 | 483 | |
C3orf38 | - | - | - |
GRCh38 GRCh37 |
2 | 14 |
CADM2 | - | - |
GRCh38 GRCh38 GRCh37 |
39 | 53 | |
CADM2-AS1 | - | - | - | GRCh38 | - | 6 |
CADM2-AS2 | - | - | - | GRCh38 | - | 7 |
CGGBP1 | - | - |
GRCh38 GRCh37 |
1 | 40 | |
CHMP2B | - | - |
GRCh38 GRCh37 |
152 | 182 | |
CNTN3 | - | - |
GRCh38 GRCh37 |
83 | 98 | |
CSNKA2IP | - | - | - | GRCh38 | - | 5 |
EPHA3 | - | - |
GRCh38 GRCh37 |
60 | 70 |
There are 116 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Jul 1, 2013 | RCV000141881.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024