ClinVar Genomic variation as it relates to human health
GRCh38/hg38 20p11.21(chr20:25485770-25612650)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 | |||
LOC121627901 | - | - | - | GRCh38 | - | 10 |
LOC125387247 | - | - | - | GRCh38 | - | 11 |
LOC126863009 | - | - | - | GRCh38 | - | 10 |
LOC130065589 | - | - | - | GRCh38 | - | 10 |
NINL | - | - |
GRCh38 GRCh37 |
101 | 138 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Feb 4, 2013 | RCV000141484.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024