ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p13.3-11(chr5:29348753-46389339)x3
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | |||
NIPBL | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
1789 | 1843 | |
FGF10 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
79 | 109 | |
DNAJC21 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
333 | 390 | |
ADAMTS12 | - | - |
GRCh38 GRCh38 GRCh37 |
86 | 150 | |
AGXT2 | - | - |
GRCh38 GRCh37 |
47 | 74 | |
AMACR | - | - |
GRCh38 GRCh37 |
2 | 440 | |
ANXA2R | - | - |
GRCh38 GRCh37 |
- | 41 | |
BRIX1 | - | - |
GRCh38 GRCh37 |
- | 53 | |
C1QTNF3 | - | - |
GRCh38 GRCh37 |
- | 55 | |
C5orf22 | - | - | - |
GRCh38 GRCh37 |
1 | 35 |
There are 63 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) |
|
May 17, 2022 | RCV002474514.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022