ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q11-12.1(chr11:55319519-56212930)x3
Germline
Classification
(1)
Benign
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 | |||
LOC126861207 | - | - | - | GRCh38 | - | 7 |
OR10AG1 | - | - | - |
GRCh38 GRCh37 |
13 | 32 |
OR4A15 | - | - | - |
GRCh38 GRCh37 |
56 | 75 |
OR4A16 | - | - | - |
GRCh38 GRCh37 |
26 | 44 |
OR4C11 | - | - | - |
GRCh38 GRCh37 |
31 | 58 |
OR4C15 | - | - | - |
GRCh38 GRCh37 |
46 | 67 |
OR4C16 | - | - | - |
GRCh38 GRCh37 |
44 | 66 |
OR4C6 | - | - | - |
GRCh38 GRCh37 |
23 | 51 |
OR4P4 | - | - | - |
GRCh38 GRCh37 |
26 | 54 |
OR4S2 | - | - | - |
GRCh38 GRCh37 |
25 | 53 |
There are 19 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Aug 12, 2011 | RCV000148269.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024