ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.4(chr11:6851550-6984119)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 | |||
OR10A2 | - | - | - |
GRCh38 GRCh37 |
23 | 44 |
OR10A4 | - | - | - |
GRCh38 GRCh37 |
16 | 37 |
OR10A5 | - | - |
GRCh38 GRCh37 |
13 | 33 | |
OR2D2 | - | - |
GRCh38 GRCh37 |
26 | 48 | |
OR2D3 | - | - | - |
GRCh38 GRCh37 |
20 | 42 |
ZNF215 | - | - |
GRCh38 GRCh37 |
37 | 61 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 1, 2019 | RCV000856656.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 23, 2024