ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11q25(chr11:132499295-134938470)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 | |||
ACAD8 | - | - |
GRCh38 GRCh37 |
254 | 354 | |
B3GAT1 | - | - |
GRCh38 GRCh37 |
11 | 107 | |
GLB1L2 | - | - | - |
GRCh38 GRCh37 |
34 | 134 |
GLB1L3 | - | - | - |
GRCh38 GRCh37 |
25 | 126 |
IGSF9B | - | - |
GRCh38 GRCh37 |
7 | 104 | |
JAM3 | - | - |
GRCh38 GRCh37 |
178 | 277 | |
LINC02714 | - | - | - |
GRCh38 GRCh37 |
3 | 106 |
LINC02743 | - | - | - |
GRCh38 GRCh37 |
- | 96 |
NCAPD3 | - | - |
GRCh38 GRCh37 |
149 | 252 | |
OPCML | - | - |
GRCh38 GRCh37 |
17 | 121 |
There are 3 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986920.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024