ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q31.2-32(chr9:109265628-117650999)
Germline
Classification
(1)
Likely 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 | |||
ZNF462 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
360 | 429 | |
ABITRAM | - | - | - |
GRCh38 GRCh37 |
10 | 58 |
ACTL7A | - | - |
GRCh38 GRCh37 |
39 | 79 | |
ACTL7B | - | - |
GRCh38 GRCh37 |
35 | 74 | |
AKNA | - | - |
GRCh38 GRCh37 |
121 | 172 | |
ALAD | - | - |
GRCh38 GRCh37 |
179 | 223 | |
AMBP | - | - |
GRCh38 GRCh37 |
34 | 70 | |
ATP6V1G1 | - | - |
GRCh38 GRCh37 |
7 | 46 | |
BSPRY | - | - |
GRCh38 GRCh37 |
33 | 74 | |
C9orf152 | - | - | - |
GRCh38 GRCh37 |
1 | 37 |
There are 53 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely pathogenic (1) |
|
Mar 1, 2022 | RCV002052828.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023