ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3p25.3(chr3:9896061-10220962)x1
Germline
Classification
(1)
Pathogenic
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 | |||
VHL | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
802 | 1957 | |
BRK1 | - | - |
GRCh38 GRCh37 |
25 | 165 | |
CRELD1 | - | - |
GRCh38 GRCh37 |
149 | 212 | |
EMC3 | - | - |
GRCh38 GRCh37 |
5 | 61 | |
EMC3-AS1 | - | - | - | GRCh38 | - | 22 |
FANCD2 | - | - |
GRCh38 GRCh37 |
93 | 1822 | |
FANCD2OS | - | - | - |
GRCh38 GRCh37 |
5 | 571 |
IL17RC | - | - |
GRCh38 GRCh37 |
609 | 727 | |
IL17RE | - | - |
GRCh38 GRCh37 |
26 | 93 | |
IRAK2 | - | - |
GRCh38 GRCh37 |
26 | 87 |
There are 26 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Nov 30, 2010 | RCV000134249.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023