ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p15.3(chr10:899498-1339873)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
ADARB2 | - | - |
GRCh38 GRCh37 |
76 | 132 | |
GTPBP4 | - | - |
GRCh38 GRCh37 |
45 | 98 | |
IDI1 | - | - |
GRCh38 GRCh37 |
5 | 59 | |
IDI2 | - | - |
GRCh38 GRCh37 |
5 | 67 | |
IDI2-AS1 | - | - | GRCh38 | - | 37 | |
LARP4B | - | - |
GRCh38 GRCh37 |
45 | 94 | |
LARP4B-DT | - | - | - | GRCh38 | - | 18 |
LINC00200 | - | - | - | GRCh38 | - | 17 |
LOC111832674 | - | - | - | GRCh38 | - | 18 |
LOC126860808 | - | - | - | GRCh38 | - | 19 |
There are 17 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000142659.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024