ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p13(chr11:33221821-34569417)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
ABTB2 | - | - | - |
GRCh38 GRCh37 |
75 | 99 |
C11orf91 | - | - | - |
GRCh38 GRCh37 |
3 | 24 |
CAPRIN1 | - | - |
GRCh38 GRCh37 |
44 | 63 | |
CAT | - | - |
GRCh38 GRCh37 |
40 | 63 | |
CD59 | - | - |
GRCh38 GRCh37 |
94 | 115 | |
ELF5 | - | - |
GRCh38 GRCh37 |
18 | 39 | |
FBXO3 | - | - |
GRCh38 GRCh37 |
17 | 38 | |
HIPK3 | - | - |
GRCh38 GRCh37 |
50 | 78 | |
KIAA1549L | - | - |
GRCh38 GRCh37 |
103 | 131 | |
LMO2 | - | - |
GRCh38 GRCh37 |
9 | 34 |
There is 1 more gene 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) |
|
Mar 16, 2019 | RCV001006402.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022