ClinVar Genomic variation as it relates to human health
NC_000005.9:g.112172610_112244011del
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 | |||
APC | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
14790 | 14927 | |
LOC112997553 | - | - | - | GRCh38 | - | 21 |
LOC126807477 | - | - | - | GRCh38 | - | 16 |
LOC129994372 | - | - | - | GRCh38 | - | 16 |
REEP5 | - | - |
GRCh38 GRCh37 |
9 | 51 | |
SRP19 | - | - |
GRCh38 GRCh37 |
6 | 52 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 1, 2002 | RCV000000855.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023