ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q35(chr7:143572320-144474990)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 | |||
ARHGEF35 | - | - | - |
GRCh38 GRCh38 GRCh37 |
34 | 92 |
ARHGEF5 | - | - |
GRCh38 GRCh38 GRCh37 |
45 | 100 | |
CTAGE4 | - | - |
GRCh38 GRCh38 GRCh37 |
26 | 82 | |
CTAGE8 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 56 |
NOBOX | - | - |
GRCh38 GRCh38 GRCh37 |
145 | 200 | |
OR2A1 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 68 |
OR2A12 | - | - | - |
GRCh38 GRCh38 GRCh37 |
11 | 71 |
OR2A14 | - | - | - |
GRCh38 GRCh38 GRCh37 |
26 | 86 |
OR2A2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
22 | 82 |
OR2A25 | - | - | - |
GRCh38 GRCh38 GRCh37 |
22 | 82 |
There are 8 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 17, 2018 | RCV000848430.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023