ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1p36.33-36.23(chr1:844347-8171914)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 | |||
CAMTA1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
580 | 686 | |
CHD5 | Little evidence for dosage pathogenicity | Not yet evaluated |
GRCh38 GRCh37 |
233 | 288 | |
GNB1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
296 | 454 | |
SKI | No evidence available | No evidence available |
GRCh38 GRCh37 |
1068 | 1212 | |
TP73 | No evidence available | No evidence available |
GRCh38 GRCh37 |
50 | 159 | |
ACAP3 | - | - | - |
GRCh38 GRCh37 |
55 | 206 |
ACOT7 | - | - |
GRCh38 GRCh37 |
26 | 86 | |
ACTRT2 | - | - |
GRCh38 GRCh37 |
27 | 165 | |
AGRN | - | - |
GRCh38 GRCh37 |
2078 | 2352 | |
AJAP1 | - | - |
GRCh38 GRCh37 |
29 | 107 |
There are 482 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) |
|
Dec 22, 2010 | RCV000136554.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 20, 2023