ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9p21.2-21.1(chr9:27348149-29866026)
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
C9orf72 | - | - |
GRCh38 GRCh37 |
95 | 177 | |
LINGO2 | - | - |
GRCh38 GRCh37 |
82 | 160 | |
MOB3B | - | - |
GRCh38 GRCh37 |
6 | 92 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2022 | RCV002053850.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022