ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q21(chr6:109780913-110202309)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 | |||
CDC40 | - | - |
GRCh38 GRCh37 |
16 | 42 | |
FIG4 | - | - |
GRCh38 GRCh37 |
982 | 1018 | |
GPR6 | - | - |
GRCh38 GRCh37 |
23 | 48 | |
LOC126859763 | - | - | - | GRCh38 | - | 10 |
LOC129996972 | - | - | - | GRCh38 | - | 11 |
LOC129996973 | - | - | - | GRCh38 | - | 11 |
LOC129996974 | - | - | - | GRCh38 | - | 11 |
LOC129996975 | - | - | - | GRCh38 | - | 11 |
WASF1 | - | - |
GRCh38 GRCh37 |
61 | 88 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 30, 2011 | RCV000140325.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023