ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q21(chr6:108531375-108589781)x1
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 | |||
FOXO3 | - | - |
GRCh38 GRCh37 |
41 | 66 | |
LOC113121302 | - | - | - | GRCh38 | - | 9 |
LOC129996942 | - | - | - | GRCh38 | - | 9 |
LOC129996943 | - | - | - | GRCh38 | - | 9 |
LOC129996944 | - | - | - | GRCh38 | - | 9 |
LOC129996945 | - | - | - | GRCh38 | - | 9 |
LOC129996946 | - | - | - | GRCh38 | - | 9 |
LOC129996947 | - | - | - | GRCh38 | - | 9 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Nov 30, 2010 | RCV000139850.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023