ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q21.3(chr10:70102749-70332271)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 | |||
DNA2 | - | - |
GRCh38 GRCh37 |
770 | 801 | |
HNRNPH3 | - | - |
GRCh38 GRCh37 |
7 | 27 | |
RUFY2 | - | - |
GRCh38 GRCh37 |
22 | 41 | |
SLC25A16 | - | - |
GRCh38 GRCh37 |
16 | 41 | |
TET1 | - | - |
GRCh38 GRCh37 |
145 | 165 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Mar 13, 2013 | RCV000737177.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 06, 2024