ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q22.1(chr7:99057038-99165274)x1
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 | |||
ATP5MF | - | - |
GRCh38 GRCh37 |
- | 29 | |
ATP5MF-PTCD1 | - | - | - |
GRCh38 GRCh37 |
- | 114 |
FAM200A | - | - | - |
GRCh38 GRCh37 |
6 | 33 |
ZKSCAN5 | - | - |
GRCh38 GRCh37 |
43 | 70 | |
ZNF394 | - | - |
GRCh38 GRCh37 |
26 | 78 | |
ZNF655 | - | - |
GRCh38 GRCh37 |
28 | 55 | |
ZNF789 | - | - | - |
GRCh38 GRCh37 |
4 | 50 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 25, 2023 | RCV003482970.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024