ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q11.1-11.2(chr3:93519764-95321276)x3
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 | |||
ARL13B | - | - |
GRCh38 GRCh37 |
332 | 381 | |
DHFR2 | - | - |
GRCh38 GRCh37 |
- | 23 | |
NSUN3 | - | - |
GRCh38 GRCh37 |
88 | 110 | |
PROS1 | - | - |
GRCh38 GRCh37 |
495 | 524 | |
STX19 | - | - | - |
GRCh38 GRCh37 |
- | 44 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 1, 2023 | RCV003885504.8 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 20, 2024