ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q34.3(chr9:137641609-138199640)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
COL5A1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2638 | 3423 | |
FCN1 | - | - |
GRCh38 GRCh37 |
33 | 80 | |
FCN2 | - | - |
GRCh38 GRCh37 |
33 | 81 | |
OLFM1 | - | - |
GRCh38 GRCh37 |
13 | 63 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 21, 2017 | RCV000683131.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022