ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q21.13(chr7:88851863-90433435)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 | |||
CDK14 | - | - |
GRCh38 GRCh37 |
30 | 51 | |
CFAP69 | - | - |
GRCh38 GRCh37 |
85 | 120 | |
CLDN12 | - | - |
GRCh38 GRCh37 |
5 | 23 | |
GTPBP10 | - | - |
GRCh38 GRCh37 |
22 | 42 | |
STEAP1 | - | - |
GRCh38 GRCh37 |
- | 63 | |
STEAP2 | - | - |
GRCh38 GRCh37 |
37 | 74 | |
ZNF804B | - | - | - |
GRCh38 GRCh37 |
93 | 141 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 29, 2022 | RCV003484690.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024