ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q32.2(chr14:100744400-100910248)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 | |||
SLC25A29 | - | - |
GRCh38 GRCh37 |
22 | 59 | |
SLC25A47 | - | - |
GRCh38 GRCh37 |
36 | 75 | |
WARS1 | - | - |
GRCh38 GRCh37 |
79 | 118 | |
WDR25 | - | - |
GRCh38 GRCh37 |
33 | 73 | |
YY1 | - | - |
GRCh38 GRCh37 |
85 | 131 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 15, 2018 | RCV000845724.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022