ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p15.32-15.2(chr5:5884444-14122539)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 | |||
CTNND2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
272 | 384 | |
ADCY2 | - | - |
GRCh38 GRCh37 |
43 | 152 | |
ANKRD33B | - | - | - |
GRCh38 GRCh37 |
45 | 151 |
ATPSCKMT | - | - |
GRCh38 GRCh37 |
15 | 117 | |
C5orf49 | - | - | - |
GRCh38 GRCh37 |
- | 7 |
CCT5 | - | - |
GRCh38 GRCh37 |
310 | 413 | |
CMBL | - | - |
GRCh38 GRCh37 |
24 | 125 | |
DAP | - | - |
GRCh38 GRCh37 |
6 | 112 | |
DNAH5 | - | - |
GRCh38 GRCh37 |
5588 | 5834 | |
FASTKD3 | - | - |
GRCh38 GRCh37 |
- | 143 |
There are 11 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) |
|
Aug 30, 2017 | RCV000682521.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022