ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q15.1(chr15:40581118-40720039)x1
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 | |||
KNL1 | - | - |
GRCh38 GRCh37 |
389 | 401 | |
LOC129390688 | - | - | - | GRCh38 | - | 1 |
LOC130056860 | - | - | - | GRCh38 | - | 1 |
LOC130056861 | - | - | - | GRCh38 | - | 1 |
LOC130056862 | - | - | - | GRCh38 | - | 1 |
LOC130056863 | - | - | - | GRCh38 | - | 1 |
LOC130056864 | - | - | - | GRCh38 | - | 3 |
RAD51 | - | - |
GRCh38 GRCh37 |
427 | 442 | |
RAD51-AS1 | - | - | - | GRCh38 | - | 1 |
TRS-GCT4-2 | - | - | - | GRCh38 | - | 1 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Jul 22, 2013 | RCV000141927.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024