ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q14.3(chr6:87564055-87921049)x3
Germline
Classification
(1)
Likely benign
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 | |||
CGA | - | - |
GRCh38 GRCh37 |
3 | 31 | |
HTR1E | - | - |
GRCh38 GRCh37 |
19 | 46 | |
ZNF292 | - | - |
GRCh38 GRCh37 |
504 | 542 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 21, 2018 | RCV001005827.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022