ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p21.3(chr9:20684175-21308693)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 | |||
FOCAD | - | - |
GRCh38 GRCh37 |
419 | 506 | |
HACD4 | - | - |
GRCh38 GRCh37 |
19 | 103 | |
IFNA10 | - | - |
GRCh38 GRCh37 |
24 | 113 | |
IFNA14 | - | - |
GRCh38 GRCh37 |
18 | 103 | |
IFNA16 | - | - |
GRCh38 GRCh37 |
13 | 100 | |
IFNA17 | - | - |
GRCh38 GRCh37 |
18 | 104 | |
IFNA21 | - | - |
GRCh38 GRCh37 |
19 | 103 | |
IFNA4 | - | - |
GRCh38 GRCh37 |
26 | 113 | |
IFNA5 | - | - |
GRCh38 GRCh37 |
14 | 97 | |
IFNA7 | - | - |
GRCh38 GRCh37 |
16 | 104 |
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) |
|
Nov 28, 2017 | RCV000847176.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022