ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.1(chr15:89738724-89788051)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 | |||
ANPEP | - | - |
GRCh38 GRCh37 |
48 | 101 | |
LOC130057888 | - | - | - | GRCh38 | - | 34 |
LOC130057889 | - | - | - | GRCh38 | - | 61 |
LOC130057890 | - | - | - | GRCh38 | - | 11 |
LOC130057891 | - | - | - | GRCh38 | - | 99 |
LOC130057892 | - | - | - | GRCh38 | - | 11 |
MESP1 | - | - |
GRCh38 GRCh37 |
9 | 131 | |
MESP2 | - | - |
GRCh38 GRCh37 |
380 | 510 | |
WDR93 | - | - |
GRCh38 GRCh37 |
18 | 70 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 27, 2013 | RCV000142209.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023