ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q31.1(chr7:111724684-112064238)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 | |||
DOCK4 | - | - |
GRCh38 GRCh37 |
129 | 194 | |
IFRD1 | - | - |
GRCh38 GRCh37 |
47 | 80 | |
ZNF277 | - | - |
GRCh38 GRCh37 |
18 | 71 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 12, 2019 | RCV001258814.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022