ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11q14.3(chr11:89062443-89762600)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 | |||
FOLH1B | - | - |
GRCh38 GRCh37 |
4 | 27 | |
NOX4 | - | - |
GRCh38 GRCh37 |
33 | 55 | |
TRIM49 | - | - |
GRCh38 GRCh37 |
28 | 55 | |
TRIM49D1 | - | - | - |
GRCh38 GRCh37 |
10 | 36 |
TRIM49D2 | - | - | - |
GRCh38 GRCh37 |
1 | 28 |
TRIM64 | - | - | - |
GRCh38 GRCh37 |
12 | 39 |
TRIM64B | - | - | - |
GRCh38 GRCh37 |
29 | 56 |
TRIM77 | - | - | - |
GRCh38 GRCh37 |
32 | 54 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 29, 2018 | RCV001006431.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023