ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5q35.2-35.3(chr5:175570677-177439550)x3
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 | |||
DDX41 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
553 | 621 | |
NSD1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1699 | 1813 | |
ARL10 | - | - | - |
GRCh38 GRCh37 |
12 | 91 |
B4GALT7 | - | - |
GRCh38 GRCh37 |
324 | 415 | |
CDHR2 | - | - |
GRCh38 GRCh37 |
110 | 168 | |
CLTB | - | - |
GRCh38 GRCh37 |
- | 57 | |
DBN1 | - | - |
GRCh38 GRCh37 |
50 | 114 | |
DOK3 | - | - |
GRCh38 GRCh37 |
52 | 126 | |
EIF4E1B | - | - | - |
GRCh38 GRCh37 |
19 | 74 |
F12 | - | - |
GRCh38 GRCh37 |
151 | 233 |
There are 28 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Mar 15, 2018 | RCV000846148.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023