ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q21.12-21.13(chr7:88148465-89871132)x3
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 | |||
STEAP1 | - | - |
GRCh38 GRCh37 |
- | 63 | |
STEAP2 | - | - |
GRCh38 GRCh37 |
37 | 74 | |
TEX47 | - | - | - |
GRCh38 GRCh37 |
- | 42 |
ZNF804B | - | - | - |
GRCh38 GRCh37 |
93 | 141 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Dec 30, 2019 | RCV001194582.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022