ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.4(chr11:4642886-5200656)x3
Germline
Classification
(1)
Likely benign
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 | |||
MMP26 | - | - |
GRCh38 GRCh37 |
20 | 313 | |
OR51A2 | - | - | - |
GRCh38 GRCh37 |
- | 44 |
OR51A4 | - | - | - |
GRCh38 GRCh37 |
- | 39 |
OR51A7 | - | - | - |
GRCh38 GRCh37 |
- | 45 |
OR51D1 | - | - | - |
GRCh38 GRCh37 |
20 | 48 |
OR51E1 | - | - |
GRCh38 GRCh37 |
27 | 55 | |
OR51E2 | - | - |
GRCh38 GRCh37 |
25 | 51 | |
OR51F1 | - | - | - |
GRCh38 GRCh37 |
- | 53 |
OR51F2 | - | - | - |
GRCh38 GRCh37 |
- | 61 |
OR51G1 | - | - | - |
GRCh38 GRCh37 |
- | 58 |
There are 9 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 |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Jun 16, 2014 | RCV000511345.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024