ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p21.3(chr9:21206361-21268920)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
IFNA10 | - | - |
GRCh38 GRCh37 |
25 | 114 | |
IFNA14 | - | - |
GRCh38 GRCh37 |
18 | 103 | |
IFNA16 | - | - |
GRCh38 GRCh37 |
17 | 104 | |
IFNA17 | - | - |
GRCh38 GRCh37 |
23 | 109 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 18, 2019 | RCV001006225.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022