ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p11.21(chr10:34766430-34894473)x3
Germline
Classification
(1)
Benign
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 | |||
LOC124403937 | - | - | - | GRCh38 | - | 6 |
LOC130003666 | - | - | - | GRCh38 | - | 6 |
LOC130003667 | - | - | - | GRCh38 | - | 6 |
LOC130003668 | - | - | - | GRCh38 | - | 6 |
LOC130003669 | - | - | - | GRCh38 | - | 6 |
LOC130003670 | - | - | - | GRCh38 | - | 6 |
PARD3 | - | - |
GRCh38 GRCh37 |
123 | 147 | |
PARD3-DT | - | - | - | GRCh38 | - | 6 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Apr 30, 2011 | RCV000140020.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023