ClinVar Genomic variation as it relates to human health
GRCh38/hg38 12p11.1(chr12:33392359-34603261)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 | |||
ALG10 | - | - |
GRCh38 GRCh37 |
43 | 78 | |
LINC02963 | - | - | - | GRCh38 | - | 11 |
LOC116268437 | - | - | - | GRCh38 | - | 14 |
LOC121832831 | - | - | - | GRCh38 | - | 11 |
LOC126861500 | - | - | - | GRCh38 | - | 12 |
LOC129390435 | - | - | - | GRCh38 | - | 11 |
LOC129390436 | - | - | - | GRCh38 | - | 11 |
LOC129390437 | - | - | - | GRCh38 | - | 11 |
LOC130007666 | - | - | - | GRCh38 | - | 11 |
LOC132090105 | - | - | - | GRCh38 | - | 11 |
There is 1 more gene 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 | RCV000142909.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024