ClinVar Genomic variation as it relates to human health
GRCh38/hg38 2q37.3(chr2:241901492-242086273)x1
Germline
Classification
(1)
Benign
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 | |||
FAM240C | - | - | - |
GRCh38 GRCh38 |
- | 44 |
LINC01237 | - | - | - |
GRCh38 GRCh38 GRCh38 GRCh38 |
2 | 92 |
LINC01238 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 69 |
LINC01880 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 68 |
LOC122889016 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 68 |
LOC132205954 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 77 |
LOC285097 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 81 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Mar 8, 2011 | RCV000136283.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024