ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q26.3(chr15:99508457-100415587)x3
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 | |||
LRRC28 | - | - | - |
GRCh38 GRCh37 |
17 | 114 |
LYSMD4 | - | - | - |
GRCh38 GRCh37 |
17 | 99 |
MEF2A | - | - |
GRCh38 GRCh37 |
41 | 131 | |
PGPEP1L | - | - | - |
GRCh38 GRCh37 |
26 | 127 |
SYNM | - | - |
GRCh38 GRCh37 |
95 | 236 | |
TTC23 | - | - | - |
GRCh38 GRCh37 |
3 | 107 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 19, 2019 | RCV001259827.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022