ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q24.3(chr15:77193423-77828917)x3
Germline
Classification
(1)
Likely 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 | |||
HMG20A | - | - |
GRCh38 GRCh37 |
24 | 47 | |
LINC00597 | - | - | - | GRCh38 | - | 6 |
LINGO1 | - | - |
GRCh38 GRCh37 |
83 | 106 | |
LINGO1-AS1 | - | - | - | GRCh38 | - | 7 |
LINGO1-AS2 | - | - | - | GRCh38 | - | 7 |
LOC101929457 | - | - | - | GRCh38 | - | 6 |
LOC112272620 | - | - | - | GRCh38 | - | 6 |
LOC121530595 | - | - | - | GRCh38 | - | 6 |
LOC121530596 | - | - | - | GRCh38 | - | 6 |
LOC129390723 | - | - | - | GRCh38 | - | 6 |
There are 9 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Sep 21, 2012 | RCV000138994.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024