ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1p36.23(chr1:7330680-7886654)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
CAMTA1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
583 | 690 | |
CAMTA1-AS1 | - | - | - | GRCh38 | - | 23 |
CAMTA1-AS2 | - | - | - | GRCh38 | - | 22 |
CAMTA1-IT1 | - | - | - | GRCh38 | - | 23 |
LOC105376689 | - | - | - | GRCh38 | - | 22 |
LOC126805602 | - | - | - | GRCh38 | - | 22 |
LOC126805603 | - | - | - | GRCh38 | - | 60 |
LOC126805604 | - | - | - | GRCh38 | - | 54 |
LOC126805605 | - | - | - | GRCh38 | - | 20 |
LOC129388431 | - | - | - | GRCh38 | - | 23 |
There are 11 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
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000051458.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 20, 2023