ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q11-12.1(chr11:55445689-57114783)x1
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 | |||
LINC02735 | - | - | - | GRCh38 | - | 3 |
LOC126861207 | - | - | - | GRCh38 | - | 7 |
LOC126861208 | - | - | - | GRCh38 | - | 3 |
LOC126861209 | - | - | - | GRCh38 | - | 3 |
MIR6128 | - | - | - |
GRCh38 GRCh38 |
- | 4 |
OR10AG1 | - | - | - |
GRCh38 GRCh37 |
13 | 32 |
OR4C11 | - | - | - |
GRCh38 GRCh37 |
31 | 58 |
OR4C15 | - | - | - |
GRCh38 GRCh37 |
46 | 67 |
OR4C16 | - | - | - |
GRCh38 GRCh37 |
44 | 66 |
OR4C6 | - | - | - |
GRCh38 GRCh37 |
23 | 51 |
There are 42 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 |
---|---|---|---|---|
Benign (1) |
|
Aug 12, 2011 | RCV000050913.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024