ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q11.1(chr6:60388301-60706083)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 | |||
LOC123744832 | - | - | - | GRCh38 | - | 5 |
LOC126088089 | - | - | - | GRCh38 | - | 6 |
LOC126088090 | - | - | - | GRCh38 | - | 6 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Nov 30, 2010 | RCV000134302.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023