ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.4(chr11:6754444-6982365)x1
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 | |||
OR10A2 | - | - | - |
GRCh38 GRCh37 |
24 | 45 |
OR10A4 | - | - | - |
GRCh38 GRCh37 |
20 | 41 |
OR10A5 | - | - |
GRCh38 GRCh37 |
16 | 36 | |
OR2AG1 | - | - | - |
GRCh38 GRCh37 |
28 | 46 |
OR2AG2 | - | - | - |
GRCh38 GRCh37 |
22 | 40 |
OR2D2 | - | - |
GRCh38 GRCh37 |
28 | 50 | |
OR2D3 | - | - | - |
GRCh38 GRCh37 |
24 | 46 |
OR6A2 | - | - |
GRCh38 GRCh37 |
28 | 46 | |
ZNF215 | - | - |
GRCh38 GRCh37 |
39 | 63 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 26, 2017 | RCV000846230.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022