ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7p22.3-21.3(chr7:45130-7252065)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 | |||
PMS2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
5177 | 5277 | |
ACTB | No evidence available | No evidence available |
GRCh38 GRCh37 |
536 | 586 | |
ADAP1 | - | - |
GRCh38 GRCh37 |
20 | 79 | |
AIMP2 | - | - |
GRCh38 GRCh37 |
71 | 208 | |
AMZ1 | - | - |
GRCh38 GRCh37 |
68 | 121 | |
ANKRD61 | - | - | - | GRCh38 | - | 18 |
AP5Z1 | - | - |
GRCh38 GRCh37 |
1021 | 1088 | |
BRAT1 | - | - |
GRCh38 GRCh37 |
1202 | 1260 | |
C1GALT1 | - | - |
GRCh38 GRCh37 |
27 | 69 | |
C7orf50 | - | - | - |
GRCh38 GRCh37 |
3 | 150 |
There are 431 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) |
|
May 19, 2011 | RCV000137524.8 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024