ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q21.33(chr9:88622823-88951838)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 | |||
C9orf153 | - | - | - |
GRCh38 GRCh37 |
- | 29 |
GOLM1 | - | - |
GRCh38 GRCh37 |
29 | 64 | |
ISCA1 | - | - |
GRCh38 GRCh37 |
23 | 63 | |
NAA35 | - | - |
GRCh38 GRCh37 |
104 | 133 | |
TUT7 | - | - |
GRCh38 GRCh37 |
67 | 96 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 8, 2018 | RCV001006242.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022