ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.5(chr11:532230-699404)x3
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 | |||
HRAS | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
9 | 708 | |
CDHR5 | - | - |
GRCh38 GRCh38 GRCh37 |
101 | 143 | |
DEAF1 | - | - |
GRCh38 GRCh38 GRCh37 |
703 | 857 | |
DRD4 | - | - |
GRCh38 GRCh38 GRCh37 |
120 | 160 | |
IRF7 | - | - |
GRCh38 GRCh38 GRCh37 |
612 | 654 | |
LMNTD2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
70 | 109 |
LMNTD2-AS1 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 39 |
LRRC56 | - | - |
GRCh38 GRCh38 GRCh37 |
340 | 1039 | |
MIR210 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 39 | |
MIR210HG | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 39 |
There are 4 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV000445988.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024