ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10p15.3(chr10:1006757-1443180)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ADARB2 | - | - |
GRCh38 GRCh37 |
84 | 140 | |
GTPBP4 | - | - |
GRCh38 GRCh37 |
46 | 100 | |
IDI1 | - | - |
GRCh38 GRCh37 |
6 | 60 | |
IDI2 | - | - |
GRCh38 GRCh37 |
5 | 68 | |
WDR37 | - | - |
GRCh38 GRCh37 |
72 | 129 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 4, 2022 | RCV003484787.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024