ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q11.23(chr7:73192369-74779057)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 | |||
ELN | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
814 | 1132 | |
GTF2I | No evidence available | No evidence available |
GRCh38 GRCh37 |
- | 178 | |
GTF2IRD1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
119 | 287 | |
LIMK1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
75 | 240 | |
NCF1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
4 | 117 | |
ABHD11 | - | - | - |
GRCh38 GRCh37 |
28 | 188 |
ABHD11-AS1 | - | - |
GRCh38 GRCh37 |
- | 159 | |
BAZ1B | - | - |
GRCh38 GRCh37 |
103 | 268 | |
BCL7B | - | - |
GRCh38 GRCh37 |
9 | 167 | |
BUD23 | - | - |
GRCh38 GRCh37 |
25 | 183 |
There are 125 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Nov 26, 2012 | RCV000138103.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024