ClinVar Genomic variation as it relates to human health
NC_000001.11:g.202057882_202124606dup
Germline
Classification
(1)
Likely benign
criteria provided, single submitter
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 | |||
GPR37L1 | - | - |
GRCh38 GRCh37 |
34 | 50 | |
LOC111429603 | - | - | - | GRCh38 | - | 3 |
LOC115804239 | - | - | - | GRCh38 | - | 3 |
LOC115804240 | - | - | - | GRCh38 | - | 3 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 1, 2018 | RCV000754398.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 07, 2023