ClinVar Genomic variation as it relates to human health
GRCh38/hg38 13q13.3(chr13:38940342-39433293)
Germline
Classification
(1)
Uncertain significance
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 | |||
LHFPL6 | - | - |
GRCh38 GRCh37 |
15 | 63 | |
LOC105370169 | - | - | - | GRCh38 | - | 26 |
LOC124855089 | - | - | - | GRCh38 | - | 27 |
LOC130009589 | - | - | - | GRCh38 | - | 26 |
LOC130009590 | - | - | - | GRCh38 | - | 26 |
LOC130009591 | - | - | - | GRCh38 | - | 26 |
LOC130009592 | - | - | - | GRCh38 | - | 25 |
LOC132090191 | - | - | - | GRCh38 | - | 28 |
LOC132090192 | - | - | - | GRCh38 | - | 28 |
LOC132090193 | - | - | - | GRCh38 | - | 28 |
There are 3 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 27, 2022 | RCV001823080.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023