ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17q24.2(chr17:68041106-68127623)x3
Germline
Classification
(1)
Likely 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 | |||
KPNA2 | - | - |
GRCh38 GRCh37 |
19 | 36 | |
LINC00674 | - | - | - | GRCh38 | - | 5 |
LOC129390922 | - | - | - | GRCh38 | - | 8 |
LOC130061504 | - | - | - | GRCh38 | - | 5 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Nov 30, 2010 | RCV000135199.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023