ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1q21.1-21.2(chr1:146872717-148353641)
Germline
Classification
(1)
Pathogenic
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 | |||
GJA5 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
217 | 573 | |
GJA8 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
236 | 523 | |
CHD1L | No evidence available | No evidence available |
GRCh38 GRCh37 |
164 | 533 | |
ACP6 | - | - |
GRCh38 GRCh37 |
33 | 320 | |
BCL9 | - | - |
GRCh38 GRCh37 |
115 | 402 | |
CH17-408M7.1 | - | - | - | GRCh38 | - | 53 |
FMO5 | - | - |
GRCh38 GRCh37 |
- | 340 | |
GPR89B | - | - |
GRCh38 GRCh37 |
10 | 287 | |
LINC00624 | - | - | - | GRCh38 | 1 | 122 |
LINC01138 | - | - | - | GRCh38 | 1 | 84 |
There are 51 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
1q21.1 microdeletion syndrome (BP3-BP4, distal)
|
Pathogenic (1) |
|
Aug 10, 2023 | RCV003448604.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 17, 2023