ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6p25.3(chr6:1989529-2084356)x1
Germline
Classification
(2)
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 | |||
GMDS | - | - |
GRCh38 GRCh37 |
25 | 118 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 2, 2019 | RCV001004815.3 | |
See cases
|
Uncertain significance (1) |
|
Sep 16, 2020 | RCV003334393.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 21, 2023