ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p21.3(chr9:20663642-21312153)x4
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 | |||
FOCAD | - | - |
GRCh38 GRCh37 |
- | - | |
HACD4 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA10 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA14 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA16 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA17 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA21 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA4 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA5 | - | - |
GRCh38 GRCh37 |
- | - | |
IFNA7 | - | - |
GRCh38 GRCh37 |
- | - |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 20, 2023 | RCV003485354.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024