ClinVar Genomic variation as it relates to human health
GRCh38/hg38 12q24.32(chr12:126526398-127998599)x3
Germline
Classification
(1)
conflicting data from submitters
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 | |||
LINC00507 | - | - | - | GRCh38 | - | 13 |
LINC00508 | - | - | - | GRCh38 | - | 14 |
LINC00943 | - | - | - | GRCh38 | - | 15 |
LINC00944 | - | - | - | GRCh38 | - | 15 |
LINC02372 | - | - | - | GRCh38 | - | 15 |
LINC02375 | - | - | - | GRCh38 | - | 15 |
LINC02376 | - | - | - | GRCh38 | - | 16 |
LINC02393 | - | - | - | GRCh38 | - | 13 |
LINC02405 | - | - | - |
GRCh38 GRCh38 |
- | 15 |
LINC02411 | - | - | - | GRCh38 | - | 14 |
There are 20 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
|
conflicting data from submitters (1) |
|
Dec 10, 2012 | RCV000139449.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024