ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p21.3(chr9:21006599-21161950)x3
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 | |||
HACD4 | - | - |
GRCh38 GRCh37 |
23 | 107 | |
IFNB1 | - | - |
GRCh38 GRCh37 |
16 | 100 | |
IFNW1 | - | - |
GRCh38 GRCh37 |
13 | 98 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 16, 2018 | RCV000848270.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022