ClinVar Genomic variation as it relates to human health
NM_001330311.2(DVL1):c.118C>G (p.Arg40Gly)
Germline
Classification
(2)
Uncertain significance
criteria provided, multiple submitters, no conflicts
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 | |||
DVL1 | - | - |
GRCh38 GRCh37 |
626 | 795 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 22, 2022 | RCV003146879.3 | |
Uncertain significance (1) |
|
Oct 4, 2023 | RCV003778868.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 17, 2024