ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8p23.1(chr8:7256134-7294303)x1
Germline
Classification
(1)
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 | |||
FAM90A13 | - | - | GRCh38 | - | 69 | |
FAM90A15 | - | - | GRCh38 | - | 69 | |
FAM90A3 | - | - | GRCh38 | - | 69 | |
FAM90A5 | - | - | GRCh38 | - | 69 | |
LINC00965 | - | - | - |
GRCh38 GRCh38 |
- | 69 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
May 30, 2010 | RCV000134019.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024