ClinVar Genomic variation as it relates to human health
GRCh37/hg19 13q34(chr13:113536131-113875644)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 | |||
ATP11A | - | - |
GRCh38 GRCh37 |
137 | 268 | |
CUL4A | - | - |
GRCh38 GRCh37 |
21 | 148 | |
F10 | - | - |
GRCh38 GRCh37 |
106 | 270 | |
F7 | - | - |
GRCh38 GRCh37 |
245 | 384 | |
MCF2L | - | - |
GRCh38 GRCh37 |
108 | 232 | |
PCID2 | - | - |
GRCh38 GRCh37 |
13 | 164 | |
PROZ | - | - |
GRCh38 GRCh37 |
23 | 175 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 17, 2020 | RCV001834277.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022