ClinVar Genomic variation as it relates to human health
GRCh38/hg38 4p16.3(chr4:78578-3363219)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 | |||
FGFR3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
943 | 1090 | |
FGFRL1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
280 | 434 | |
LETM1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
248 | 392 | |
NELFA | No evidence available | No evidence available |
GRCh38 GRCh37 |
67 | 215 | |
NSD2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
461 | 609 | |
ADD1 | - | - |
GRCh38 GRCh37 |
43 | 168 | |
ATP5ME | - | - |
GRCh38 GRCh37 |
7 | 165 | |
CFAP99 | - | - | - | GRCh38 | 62 | 132 |
CPLX1 | - | - |
GRCh38 GRCh37 |
67 | 222 | |
CRIPAK | - | - |
GRCh38 GRCh37 |
- | 239 |
There are 248 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 30, 2010 | RCV000135317.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023