ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17q21.31(chr17:46322082-46685236)x1
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 | |||
ARL17A | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 115 |
ARL17B | - | - | - |
GRCh38 GRCh37 |
2 | 108 |
FAM215B | - | - | - |
GRCh38 GRCh38 |
- | 31 |
LOC112533643 | - | - | - |
GRCh38 GRCh38 |
- | 32 |
LRRC37A | - | - |
GRCh38 GRCh38 GRCh37 |
- | 115 | |
LRRC37A2 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
- | 645 | |
NSF | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
1 | 63 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Sep 21, 2012 | RCV000139705.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024