ClinVar Genomic variation as it relates to human health
GRCh37/hg19 13q33.1-33.3(chr13:103694735-109007552)x1
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ABHD13 | - | - | - |
GRCh38 GRCh37 |
16 | 133 |
ARGLU1 | - | - |
GRCh38 GRCh37 |
10 | 120 | |
DAOA | - | - |
GRCh38 GRCh37 |
- | 125 | |
DAOA-AS1 | - | - |
GRCh38 GRCh37 |
- | 125 | |
EFNB2 | - | - |
GRCh38 GRCh37 |
9 | 128 | |
LIG4 | - | - |
GRCh38 GRCh37 |
699 | 816 | |
NALF1 | - | - |
GRCh38 GRCh37 |
33 | 153 | |
SLC10A2 | - | - |
GRCh38 GRCh37 |
295 | 398 | |
TNFSF13B | - | - |
GRCh38 GRCh37 |
6 | 126 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003987025.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024