ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q33-34(chr7:137848980-138897699)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
ATP6V0A4 | - | - |
GRCh38 GRCh37 |
413 | 483 | |
KIAA1549 | - | - |
GRCh38 GRCh37 |
1413 | 1460 | |
SVOPL | - | - |
GRCh38 GRCh37 |
61 | 106 | |
TMEM213 | - | - | - |
GRCh38 GRCh37 |
8 | 68 |
TRIM24 | - | - |
GRCh38 GRCh37 |
33 | 88 | |
TTC26 | - | - |
GRCh38 GRCh37 |
- | 4 | |
ZC3HAV1 | - | - |
GRCh38 GRCh37 |
58 | 105 | |
ZC3HAV1L | - | - | - |
GRCh38 GRCh37 |
15 | 62 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 16, 2017 | RCV000846058.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022