ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q13(chr6:73881985-74138519)x3
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 | |||
CGAS | - | - |
GRCh38 GRCh37 |
25 | 48 | |
DDX43 | - | - |
GRCh38 GRCh37 |
37 | 51 | |
DPPA5 | - | - |
GRCh38 GRCh37 |
5 | 19 | |
KCNQ5 | - | - |
GRCh38 GRCh37 |
535 | 677 | |
KHDC1 | - | - |
GRCh38 GRCh37 |
- | 37 | |
KHDC1L | - | - | - |
GRCh38 GRCh37 |
- | 20 |
KHDC3L | - | - |
GRCh38 GRCh37 |
28 | 42 | |
OOEP | - | - |
GRCh38 GRCh37 |
7 | 27 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 30, 2018 | RCV001005813.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 11, 2024