ClinVar Genomic variation as it relates to human health
GRCh37/hg19 8q24.3(chr8:145899733-146107871)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 | |||
COMMD5 | - | - |
GRCh38 GRCh37 |
11 | 101 | |
RPL8 | - | - |
GRCh38 GRCh37 |
13 | 78 | |
ZNF250 | - | - | - |
GRCh38 GRCh37 |
21 | 81 |
ZNF251 | - | - | - |
GRCh38 GRCh38 GRCh37 |
37 | 102 |
ZNF34 | - | - |
GRCh38 GRCh37 |
26 | 89 | |
ZNF517 | - | - | - |
GRCh38 GRCh37 |
47 | 109 |
ZNF7 | - | - |
GRCh38 GRCh37 |
8 | 97 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 17, 2022 | RCV002473766.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023