ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q36.1(chr7:149964361-150163624)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 | |||
ACTR3C | - | - | - |
GRCh38 GRCh37 |
22 | 93 |
GIMAP8 | - | - |
GRCh38 GRCh37 |
32 | 125 | |
LRRC61 | - | - | - |
GRCh38 GRCh37 |
21 | 99 |
RARRES2 | - | - |
GRCh38 GRCh37 |
10 | 79 | |
REPIN1 | - | - |
GRCh38 GRCh37 |
- | 114 | |
ZBED6CL | - | - |
GRCh38 GRCh37 |
- | 78 | |
ZNF775 | - | - | - |
GRCh38 GRCh37 |
53 | 123 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 21, 2017 | RCV000849576.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022